Linked Data
ClinVar Variation Id:
712150
ClinVar RCV Id:
RCV000884037
dbSNP Id:
rs111241221
ExAC:
14:101347762 G / A
gnomAD v2:
14-101347762-G-A
gnomAD v3:
14-100881425-G-A
gnomAD v4:
14-100881425-G-A
COSMIC:
COSM4243355
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100881425G>A , CM000676.2:g.100881425G>A | GRCh38 |
| NC_000014.8:g.101347762G>A , CM000676.1:g.101347762G>A | GRCh37 |
| NC_000014.7:g.100417515G>A | NCBI36 |
| NG_045001.1:g.8423C>T | |
| NG_045000.5:g.50157G>A | |
| NG_045000.6:g.50157G>A | |
| NG_045001.2:g.27298C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649591.1:c.3364C>T MANE Select | ENSP00000497482.1:p.Arg1122Cys | |
| ENST00000534062.1:c.3364C>T | ENSP00000435342.1:p.Arg1122Cys | |
| NM_001134888.2:c.3364C>T | NP_001128360.1:p.Arg1122Cys | |
| NM_001134888.3:c.3364C>T MANE Select | NP_001128360.1:p.Arg1122Cys |