Linked Data
ClinVar Variation Id:
1102382
ClinVar RCV Id:
RCV001425679
dbSNP Id:
rs782518797
ExAC:
X:153001577 G / A
gnomAD v2:
X-153001577-G-A
gnomAD v3:
X-153736123-G-A
gnomAD v4:
X-153736123-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153736123G>A , CM000685.2:g.153736123G>A | GRCh38 |
| NC_000023.10:g.153001577G>A , CM000685.1:g.153001577G>A | GRCh37 |
| NC_000023.9:g.152654771G>A | NCBI36 |
| NG_009022.2:g.16256G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1093G>A MANE Select | ENSP00000218104.3:p.Val365Met | |
| ENST00000218104.5:c.1093G>A | ENSP00000218104.3:p.Val365Met | |
| ENST00000443684.2:n.96G>A | ||
| NM_000033.3:c.1093G>A | NP_000024.2:p.Val365Met | |
| XR_938507.1:n.1509G>A | ||
| XR_938507.2:n.1509G>A | ||
| NM_000033.4:c.1093G>A MANE Select | NP_000024.2:p.Val365Met |