Linked Data
ClinVar Variation Id:
301572
dbSNP Id:
rs550415126
ExAC:
10:90974759 C / T
gnomAD v2:
10-90974759-C-T
gnomAD v3:
10-89215002-C-T
gnomAD v4:
10-89215002-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.89215002C>T , CM000672.2:g.89215002C>T | GRCh38 |
| NC_000010.10:g.90974759C>T , CM000672.1:g.90974759C>T | GRCh37 |
| NC_000010.9:g.90964739C>T | NCBI36 |
| NG_008194.1:g.41902G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336233.10:c.1026G>A MANE Select | ENSP00000337354.5:p.Gly342= | |
| ENST00000336233.9:c.1026G>A | ENSP00000337354.5:p.Gly342= | |
| ENST00000371837.5:c.858G>A | ENSP00000360903.1:p.Gly286= | |
| ENST00000456827.5:c.678G>A | ENSP00000413019.2:p.Gly226= | |
| NM_000235.3:c.1026G>A | NP_000226.2:p.Gly342= | |
| NM_001127605.2:c.1026G>A | NP_001121077.1:p.Gly342= | |
| NM_001288979.1:c.678G>A | NP_001275908.1:p.Gly226= | |
| XM_024448023.1:c.1026G>A | XP_024303791.1:p.Gly342= | |
| NM_000235.4:c.1026G>A MANE Select | NP_000226.2:p.Gly342= | |
| NM_001127605.3:c.1026G>A | NP_001121077.1:p.Gly342= | |
| NM_001288979.2:c.678G>A | NP_001275908.1:p.Gly226= |