Linked Data
ClinVar Variation Id:
6466
dbSNP Id:
rs61752117
gnomAD v2:
11-45936170-G-A
gnomAD v3:
11-45914619-G-A
gnomAD v4:
11-45914619-G-A
PubMed:
PMID:9837814
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.45914619G>A , CM000673.2:g.45914619G>A | GRCh38 |
| NC_000011.9:g.45936170G>A , CM000673.1:g.45936170G>A | GRCh37 |
| NC_000011.8:g.45892746G>A | NCBI36 |
| NG_008460.1:g.8505C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378750.10:c.526C>T MANE Select | ENSP00000368024.5:p.Arg176Ter | |
| ENST00000241041.7:c.526C>T | ENSP00000241041.3:p.Arg176Ter | |
| ENST00000378750.9:c.526C>T | ENSP00000368024.5:p.Arg176Ter | |
| ENST00000525192.5:c.241C>T | ENSP00000431309.1:p.Arg81Ter | |
| ENST00000527371.1:n.142C>T | ||
| ENST00000532554.5:n.297C>T | ||
| ENST00000532681.5:c.241C>T | ENSP00000434654.1:p.Arg81Ter | |
| ENST00000533151.5:c.214C>T | ENSP00000433045.1:p.Arg72Ter | |
| NM_004813.2:c.526C>T | NP_004804.1:p.Arg176Ter | |
| NM_057174.2:c.526C>T | NP_476515.1:p.Arg176Ter | |
| XM_011520474.1:c.403C>T | XP_011518776.1:p.Arg135Ter | |
| NM_004813.3:c.526C>T | NP_004804.1:p.Arg176Ter | |
| NM_004813.4:c.526C>T MANE Select | NP_004804.2:p.Arg176Ter | |
| NM_057174.3:c.526C>T | NP_476515.2:p.Arg176Ter |