Linked Data
ClinVar Variation Id:
1052705
ClinVar RCV Id:
RCV001360936
dbSNP Id:
rs1186145382
gnomAD v2:
19-18898403-C-T
gnomAD v3:
19-18787594-C-T
gnomAD v4:
19-18787594-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18787594C>T , CM000681.2:g.18787594C>T | GRCh38 |
| NC_000019.9:g.18898403C>T , CM000681.1:g.18898403C>T | GRCh37 |
| NC_000019.8:g.18759403C>T | NCBI36 |
| NG_007070.1:g.8712G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1032G>A MANE Select | ENSP00000222271.2:p.Trp344Ter | |
| ENST00000222271.6:c.1032G>A | ENSP00000222271.2:p.Trp344Ter | |
| ENST00000425807.1:c.873G>A | ENSP00000403792.1:p.Trp291Ter | |
| ENST00000542601.6:c.933G>A | ENSP00000439156.2:p.Trp311Ter | |
| NM_000095.2:c.1032G>A | NP_000086.2:p.Trp344Ter | |
| NM_000095.3:c.1032G>A MANE Select | NP_000086.2:p.Trp344Ter |