Linked Data
ClinVar Variation Id:
2875645
ClinVar RCV Id:
RCV003654532
dbSNP Id:
rs2058956309
gnomAD v4:
3-12604235-G-C
MyVariant Identifiers:
chr3:g.12645734G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12604235G>C , CM000665.2:g.12604235G>C | GRCh38 |
| NC_000003.11:g.12645734G>C , CM000665.1:g.12645734G>C | GRCh37 |
| NC_000003.10:g.12620734G>C | NCBI36 |
| NG_007467.1:g.64945C>G , LRG_413:g.64945C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000416093.2:c.*412C>G | ENSP00000391265.2:n.*412C>G | |
| ENST00000423275.6:c.*412C>G | ENSP00000401088.1:n.*412C>G | |
| ENST00000432427.3:c.55C>G | ||
| ENST00000465826.6:n.326C>G | ||
| ENST00000491290.2:n.1112C>G | ||
| ENST00000684903.1:c.*412C>G | ENSP00000508612.1:n.*412C>G | |
| ENST00000685348.1:c.*412C>G | ENSP00000510285.1:n.*412C>G | |
| ENST00000685437.1:c.636C>G | ENSP00000508794.1:p.Pro212= | |
| ENST00000685653.1:c.735C>G | ENSP00000509968.1:p.Pro245= | |
| ENST00000685738.1:c.735C>G | ENSP00000510156.1:p.Pro245= | |
| ENST00000685959.1:c.735C>G | ENSP00000510452.1:p.Pro245= | |
| ENST00000686409.1:n.1335C>G | ||
| ENST00000686455.1:n.1098C>G | ||
| ENST00000686479.1:n.1106C>G | ||
| ENST00000686762.1:c.735C>G | ENSP00000509767.1:p.Pro245= | |
| ENST00000687257.1:n.971C>G | ||
| ENST00000687326.1:c.735C>G | ENSP00000509665.1:p.Pro245= | |
| ENST00000687486.1:c.55C>G | ||
| ENST00000687505.1:n.853C>G | ||
| ENST00000687923.1:c.636C>G | ENSP00000510255.1:p.Pro212= | |
| ENST00000687940.1:n.1112C>G | ||
| ENST00000688269.1:n.1343C>G | ||
| ENST00000688326.1:c.55C>G | ||
| ENST00000688444.1:n.1061C>G | ||
| ENST00000688543.1:c.636C>G | ENSP00000509612.1:p.Pro212= | |
| ENST00000688625.1:c.*313C>G | ENSP00000509522.1:n.*313C>G | |
| ENST00000688803.1:n.966C>G | ||
| ENST00000689033.1:c.735C>G | ENSP00000508983.1:p.Pro245= | |
| ENST00000689097.1:c.*412C>G | ENSP00000509756.1:n.*412C>G | |
| ENST00000689389.1:c.735C>G | ENSP00000510213.1:p.Pro245= | |
| ENST00000689418.1:c.*412C>G | ENSP00000509467.1:n.*412C>G | |
| ENST00000689481.1:c.*412C>G | ENSP00000510248.1:n.*412C>G | |
| ENST00000689540.1:n.885C>G | ||
| ENST00000689876.1:c.735C>G | ENSP00000508535.1:p.Pro245= | |
| ENST00000689914.1:c.735C>G | ENSP00000509847.1:p.Pro245= | |
| ENST00000690397.1:c.636C>G | ENSP00000508730.1:p.Pro212= | |
| ENST00000690460.1:c.735C>G | ENSP00000509106.1:p.Pro245= | |
| ENST00000690625.1:n.1038C>G | ||
| ENST00000691268.1:c.262-3820C>G | ||
| ENST00000691396.1:c.*528C>G | ENSP00000510712.1:n.*528C>G | |
| ENST00000691724.1:c.735C>G | ENSP00000509255.1:p.Pro245= | |
| ENST00000691779.1:c.*313C>G | ENSP00000508592.1:n.*313C>G | |
| ENST00000691899.1:c.735C>G | ENSP00000508763.1:p.Pro245= | |
| ENST00000692093.1:c.636C>G | ENSP00000509669.1:p.Pro212= | |
| ENST00000692311.1:n.1108C>G | ||
| ENST00000692558.1:n.1100C>G | ||
| ENST00000692773.1:c.*412C>G | ENSP00000509055.1:n.*412C>G | |
| ENST00000692830.1:c.*480C>G | ENSP00000509461.1:n.*480C>G | |
| ENST00000693069.1:c.636C>G | ENSP00000510072.1:p.Pro212= | |
| ENST00000693312.1:c.510C>G | ENSP00000508686.1:p.Pro170= | |
| ENST00000693664.1:c.735C>G | ENSP00000509614.1:p.Pro245= | |
| ENST00000693705.1:c.*412C>G | ENSP00000510697.1:n.*412C>G | |
| ENST00000251849.9:c.735C>G MANE Select | ENSP00000251849.4:p.Pro245= | |
| ENST00000442415.7:c.735C>G | ENSP00000401888.2:p.Pro245= | |
| ENST00000251849.8:c.735C>G | ENSP00000251849.4:p.Pro245= | |
| ENST00000416093.1:c.*313C>G | ENSP00000391265.1:n.*313C>G | |
| ENST00000423275.5:c.*412C>G | ENSP00000401088.1:n.*412C>G | |
| ENST00000432427.2:c.372C>G | ENSP00000398591.2:p.Pro124= | |
| ENST00000442415.6:c.735C>G | ENSP00000401888.2:p.Pro245= | |
| ENST00000491290.1:n.256C>G | ||
| NM_002880.3:c.735C>G , LRG_413t1:c.735C>G | NP_002871.1:p.Pro245= | |
| XM_005265355.1:c.735C>G | XP_005265412.1:p.Pro245= | |
| XM_005265357.1:c.636C>G | XP_005265414.1:p.Pro212= | |
| XM_005265358.3:c.492C>G | XP_005265415.1:p.Pro164= | |
| XM_005265359.3:c.393C>G | XP_005265416.1:p.Pro131= | |
| XM_005265360.1:c.735C>G | XP_005265417.1:p.Pro245= | |
| XM_011533974.1:c.735C>G | XP_011532276.1:p.Pro245= | |
| XM_011533975.1:c.492C>G | XP_011532277.1:p.Pro164= | |
| NM_001354689.1:c.735C>G | NP_001341618.1:p.Pro245= | |
| NM_001354690.1:c.735C>G | NP_001341619.1:p.Pro245= | |
| NM_001354691.1:c.492C>G | NP_001341620.1:p.Pro164= | |
| NM_001354692.1:c.492C>G | NP_001341621.1:p.Pro164= | |
| NM_001354693.1:c.636C>G | NP_001341622.1:p.Pro212= | |
| NM_001354694.1:c.492C>G | NP_001341623.1:p.Pro164= | |
| NM_001354695.1:c.393C>G | NP_001341624.1:p.Pro131= | |
| NR_148940.1:n.1150C>G | ||
| NR_148941.1:n.1150C>G | ||
| NR_148942.1:n.1150C>G | ||
| XM_011533974.3:c.735C>G | XP_011532276.1:p.Pro245= | |
| XM_017006966.1:c.636C>G | XP_016862455.1:p.Pro212= | |
| XR_001740227.1:n.967C>G | ||
| NM_001354689.3:c.735C>G | NP_001341618.1:p.Pro245= | |
| NM_001354690.2:c.735C>G | NP_001341619.1:p.Pro245= | |
| NM_001354691.2:c.492C>G | NP_001341620.1:p.Pro164= | |
| NM_001354692.2:c.492C>G | NP_001341621.1:p.Pro164= | |
| NM_001354693.2:c.636C>G | NP_001341622.1:p.Pro212= | |
| NM_001354694.2:c.492C>G | NP_001341623.1:p.Pro164= | |
| NM_001354695.2:c.393C>G | NP_001341624.1:p.Pro131= | |
| NR_148940.2:n.1066C>G | ||
| NR_148941.2:n.1066C>G | ||
| NR_148942.2:n.1066C>G | ||
| NM_001354690.3:c.735C>G | NP_001341619.1:p.Pro245= | |
| NM_001354691.3:c.492C>G | NP_001341620.1:p.Pro164= | |
| NM_001354692.3:c.492C>G | NP_001341621.1:p.Pro164= | |
| NM_001354693.3:c.636C>G | NP_001341622.1:p.Pro212= | |
| NM_001354694.3:c.492C>G | NP_001341623.1:p.Pro164= | |
| NM_001354695.3:c.393C>G | NP_001341624.1:p.Pro131= | |
| NM_002880.4:c.735C>G MANE Select | NP_002871.1:p.Pro245= | |
| NR_148940.3:n.1066C>G | ||
| NR_148941.3:n.1066C>G | ||
| NR_148942.3:n.1066C>G |