Linked Data
ClinVar Variation Id:
521662
ClinVar RCV Id:
RCV000623594
dbSNP Id:
rs1556055232
gnomAD v4:
X-25013150-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25013150A>T , CM000685.2:g.25013150A>T | GRCh38 |
| NC_000023.10:g.25031267A>T , CM000685.1:g.25031267A>T | GRCh37 |
| NC_000023.9:g.24941188A>T | NCBI36 |
| NG_008281.1:g.7799T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.845T>A MANE Select | ENSP00000368332.4:p.Val282Glu | |
| ENST00000379044.4:c.845T>A | ENSP00000368332.4:p.Val282Glu | |
| NM_139058.2:c.845T>A | NP_620689.1:p.Val282Glu | |
| NM_139058.3:c.845T>A MANE Select | NP_620689.1:p.Val282Glu |