Linked Data
ClinVar Variation Id:
8246
dbSNP Id:
rs121909285
gnomAD v4:
12-51913187-G-T
PubMed:
PMID:9245985
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51913187G>T , CM000674.2:g.51913187G>T | GRCh38 |
| NC_000012.11:g.52306971G>T , CM000674.1:g.52306971G>T | GRCh37 |
| NC_000012.10:g.50593238G>T | NCBI36 |
| NG_009549.1:g.10770G>T , LRG_543:g.10770G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000547400.6:c.192G>T | ENSP00000446724.2:p.Trp64Cys | |
| ENST00000551576.6:c.150G>T | ENSP00000455848.2:p.Trp50Cys | |
| ENST00000552678.2:c.150G>T | ENSP00000457394.2:p.Trp50Cys | |
| ENST00000388922.9:c.150G>T MANE Select | ENSP00000373574.4:p.Trp50Cys | |
| ENST00000388922.8:c.150G>T | ENSP00000373574.4:p.Trp50Cys | |
| ENST00000419526.6:c.103+652G>T | ENSP00000392492.2:n.103+652G>T | |
| ENST00000547400.5:c.192G>T | ENSP00000446724.1:p.Trp64Cys | |
| ENST00000550683.5:c.192G>T | ENSP00000447884.1:p.Trp64Cys | |
| ENST00000551576.5:c.150G>T | ENSP00000455848.1:p.Trp50Cys | |
| NM_000020.2:c.150G>T , LRG_543t1:c.150G>T | NP_000011.2:p.Trp50Cys | |
| NM_001077401.1:c.150G>T | NP_001070869.1:p.Trp50Cys | |
| XM_005269235.2:c.150G>T | XP_005269292.1:p.Trp50Cys | |
| XM_011539008.1:c.192G>T | XP_011537310.1:p.Trp64Cys | |
| NM_000020.3:c.150G>T MANE Select | NP_000011.2:p.Trp50Cys | |
| NM_001077401.2:c.150G>T | NP_001070869.1:p.Trp50Cys |