Linked Data
ClinVar Variation Id:
2728132
dbSNP Id:
rs369210624
ExAC:
10:124266338 C / T
gnomAD v2:
10-124266338-C-T
gnomAD v3:
10-122506822-C-T
gnomAD v4:
10-122506822-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506822C>T , CM000672.2:g.122506822C>T | GRCh38 |
| NC_000010.10:g.124266338C>T , CM000672.1:g.124266338C>T | GRCh37 |
| NC_000010.9:g.124256328C>T | NCBI36 |
| NG_011554.1:g.50298C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.909C>T MANE Select | ENSP00000357980.3:p.Gly303= | |
| ENST00000648167.1:c.591C>T | ENSP00000498033.1:p.Gly197= | |
| ENST00000368984.7:c.909C>T | ENSP00000357980.3:p.Gly303= | |
| ENST00000420892.1:c.132C>T | ENSP00000412676.1:p.Gly44= | |
| NM_002775.4:c.909C>T | NP_002766.1:p.Gly303= | |
| NM_002775.5:c.909C>T MANE Select | NP_002766.1:p.Gly303= |