Linked Data
ClinVar Variation Id:
1660302
ClinVar RCV Id:
RCV002183629
dbSNP Id:
rs2146361304
MyVariant Identifiers:
chr21:g.36252897A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34880600A>C , CM000683.2:g.34880600A>C | GRCh38 |
| NC_000021.8:g.36252897A>C , CM000683.1:g.36252897A>C | GRCh37 |
| NC_000021.7:g.35174767A>C | NCBI36 |
| NG_011402.2:g.1109112T>G , LRG_482:g.1109112T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000675419.1:c.465T>G MANE Select | ENSP00000501943.1:p.Val155= | |
| ENST00000300305.7:c.465T>G | ENSP00000300305.3:p.Val155= | |
| ENST00000344691.8:c.384T>G | ENSP00000340690.4:p.Val128= | |
| ENST00000358356.9:c.384T>G | ENSP00000351123.5:p.Val128= | |
| ENST00000399237.6:c.429T>G | ENSP00000382182.2:p.Val143= | |
| ENST00000399240.5:c.384T>G | ENSP00000382184.1:p.Val128= | |
| ENST00000437180.5:c.465T>G | ENSP00000409227.1:p.Val155= | |
| ENST00000482318.5:c.*55T>G | ENSP00000477067.1:n.*55T>G | |
| NM_001001890.2:c.384T>G | NP_001001890.1:p.Val128= | |
| NM_001122607.1:c.384T>G | NP_001116079.1:p.Val128= | |
| NM_001754.4:c.465T>G , LRG_482t1:c.465T>G | NP_001745.2:p.Val155= | |
| XM_005261068.3:c.429T>G | XP_005261125.1:p.Val143= | |
| XM_005261069.3:c.465T>G | XP_005261126.1:p.Val155= | |
| XM_011529766.1:c.465T>G | XP_011528068.1:p.Val155= | |
| XM_011529767.1:c.426T>G | XP_011528069.1:p.Val142= | |
| XM_011529768.1:c.426T>G | XP_011528070.1:p.Val142= | |
| XM_011529770.1:c.465T>G | XP_011528072.1:p.Val155= | |
| XR_937576.1:n.644T>G | ||
| XM_005261069.4:c.465T>G | XP_005261126.1:p.Val155= | |
| XM_011529766.2:c.465T>G | XP_011528068.1:p.Val155= | |
| XM_011529767.2:c.426T>G | XP_011528069.1:p.Val142= | |
| XM_011529768.2:c.426T>G | XP_011528070.1:p.Val142= | |
| XM_011529770.2:c.465T>G | XP_011528072.1:p.Val155= | |
| XM_017028487.1:c.312T>G | XP_016883976.1:p.Val104= | |
| XR_937576.2:n.691T>G | ||
| NM_001001890.3:c.384T>G | NP_001001890.1:p.Val128= | |
| NM_001122607.2:c.384T>G | NP_001116079.1:p.Val128= | |
| NM_001754.5:c.465T>G MANE Select | NP_001745.2:p.Val155= |