Linked Data
ClinVar Variation Id:
989603
ClinVar RCV Id:
RCV001277469
dbSNP Id:
rs745748793
ExAC:
13:20763036 T / C
gnomAD v2:
13-20763036-T-C
gnomAD v3:
13-20188897-T-C
gnomAD v4:
13-20188897-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20188897T>C , CM000675.2:g.20188897T>C | GRCh38 |
| NC_000013.10:g.20763036T>C , CM000675.1:g.20763036T>C | GRCh37 |
| NC_000013.9:g.19661036T>C | NCBI36 |
| NG_008358.1:g.9079A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.*4A>G | ENSP00000372295.1:n.*4A>G | |
| ENST00000382848.5:c.*4A>G MANE Select | ENSP00000372299.4:n.*4A>G | |
| ENST00000382844.1:c.*4A>G | ENSP00000372295.1:n.*4A>G | |
| ENST00000382848.4:c.*4A>G | ENSP00000372299.4:n.*4A>G | |
| NM_004004.5:c.*4A>G | NP_003995.2:n.*4A>G | |
| XM_011535049.1:c.*4A>G | XP_011533351.1:n.*4A>G | |
| XM_011535049.2:c.*4A>G | XP_011533351.1:n.*4A>G | |
| NM_004004.6:c.*4A>G MANE Select | NP_003995.2:n.*4A>G |