Linked Data
ClinVar Variation Id:
343456
ClinVar RCV Id:
RCV000348610
dbSNP Id:
rs754664563
ExAC:
3:135969262 C / T
gnomAD v2:
3-135969262-C-T
gnomAD v4:
3-136250420-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.136250420C>T , CM000665.2:g.136250420C>T | GRCh38 |
| NC_000003.11:g.135969262C>T , CM000665.1:g.135969262C>T | GRCh37 |
| NC_000003.10:g.137451952C>T | NCBI36 |
| NG_008939.1:g.5096C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251654.9:c.45C>T MANE Select | ENSP00000251654.4:p.Ser15= | |
| ENST00000251654.8:c.45C>T | ENSP00000251654.4:p.Ser15= | |
| ENST00000462637.5:c.45C>T | ENSP00000420391.1:p.Ser15= | |
| ENST00000465423.5:c.45C>T | ENSP00000419263.1:p.Ser15= | |
| ENST00000466072.5:c.45C>T | ENSP00000420158.1:p.Ser15= | |
| ENST00000468777.5:c.45C>T | ENSP00000419129.1:p.Ser15= | |
| ENST00000469217.5:c.45C>T | ENSP00000419027.1:p.Ser15= | |
| ENST00000471595.5:c.45C>T | ENSP00000417549.1:p.Ser15= | |
| ENST00000474833.5:n.30C>T | ||
| ENST00000478469.5:c.45C>T | ENSP00000420759.1:p.Ser15= | |
| ENST00000482086.5:c.45C>T | ENSP00000417253.1:p.Ser15= | |
| ENST00000483687.5:c.45C>T | ENSP00000420639.1:p.Ser15= | |
| ENST00000484181.5:c.45C>T | ENSP00000417937.1:p.Ser15= | |
| ENST00000490504.5:c.45C>T | ENSP00000418307.1:p.Ser15= | |
| NM_000532.4:c.45C>T | NP_000523.2:p.Ser15= | |
| NM_001178014.1:c.45C>T | NP_001171485.1:p.Ser15= | |
| XM_011512873.1:c.45C>T | XP_011511175.1:p.Ser15= | |
| XM_011512873.2:c.45C>T | XP_011511175.1:p.Ser15= | |
| NM_000532.5:c.45C>T MANE Select | NP_000523.2:p.Ser15= | |
| NM_001178014.2:c.45C>T | NP_001171485.1:p.Ser15= |