Linked Data
ClinVar Variation Id:
127188
ClinVar RCV Id:
RCV000115017
dbSNP Id:
rs587777354
PubMed:
PMID:23650303
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431559C>A , CM000663.2:g.229431559C>A | GRCh38 |
| NC_000001.10:g.229567306C>A , CM000663.1:g.229567306C>A | GRCh37 |
| NC_000001.9:g.227633929C>A | NCBI36 |
| NG_006672.1:g.7538G>T , LRG_429:g.7538G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.996G>T | ENSP00000355644.4:p.Trp332Cys | |
| ENST00000684723.1:c.939G>T | ENSP00000508084.1:p.Trp313Cys | |
| ENST00000366683.3:c.705G>T | ENSP00000355644.3:p.Trp235Cys | |
| ENST00000366684.7:c.1074G>T MANE Select | ENSP00000355645.3:p.Trp358Cys | |
| NM_001100.3:c.1074G>T , LRG_429t1:c.1074G>T | NP_001091.1:p.Trp358Cys | |
| NM_001100.4:c.1074G>T MANE Select | NP_001091.1:p.Trp358Cys |