Linked Data
ClinVar Variation Id:
298628
ClinVar RCV Id:
RCV000267824
dbSNP Id:
rs140012815
ExAC:
10:104597133 G / A
gnomAD v2:
10-104597133-G-A
gnomAD v3:
10-102837376-G-A
gnomAD v4:
10-102837376-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102837376G>A , CM000672.2:g.102837376G>A | GRCh38 |
| NC_000010.10:g.104597133G>A , CM000672.1:g.104597133G>A | GRCh37 |
| NC_000010.9:g.104587123G>A | NCBI36 |
| NG_007955.1:g.5158C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369887.4:c.-15C>T MANE Select | ENSP00000358903.3:n.-15C>T | |
| ENST00000638190.1:c.-15C>T | ENSP00000492539.1:n.-15C>T | |
| ENST00000638272.1:c.-15C>T | ENSP00000491508.1:n.-15C>T | |
| ENST00000638971.1:c.-15C>T | ENSP00000492313.1:n.-15C>T | |
| ENST00000639393.1:c.-15C>T | ENSP00000492651.1:n.-15C>T | |
| ENST00000369887.3:c.-15C>T | ENSP00000358903.3:n.-15C>T | |
| ENST00000489268.1:n.39C>T | ||
| NM_000102.3:c.-15C>T | NP_000093.1:n.-15C>T | |
| NM_000102.4:c.-15C>T MANE Select | NP_000093.1:n.-15C>T |