Linked Data
dbSNP Id:
rs926001644
gnomAD v4:
X-119930221-G-A
MyVariant Identifiers:
chrX:g.119930221G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.119930221G>A , CM000685.2:g.119930221G>A | GRCh38 |
| NC_000023.10:g.119064184G>A , CM000685.1:g.119064184G>A | GRCh37 |
| NC_000023.9:g.118948212G>A | NCBI36 |
| NG_021260.1:g.18552C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371410.5:c.924-56C>T MANE Select | ENSP00000360464.3:n.924-56C>T | |
| ENST00000652253.1:c.920-56C>T | ||
| ENST00000371410.4:c.924-56C>T | ENSP00000360464.3:n.924-56C>T | |
| ENST00000477789.5:n.1852-56C>T | ||
| ENST00000482407.1:n.723-56C>T | ||
| NM_024528.3:c.924-56C>T | NP_078804.2:n.924-56C>T | |
| XM_017029842.1:c.627-56C>T | XP_016885331.1:n.627-56C>T | |
| NM_024528.4:c.924-56C>T MANE Select | NP_078804.2:n.924-56C>T |