Linked Data
dbSNP Id:
rs750074228
gnomAD v4:
X-25004645-G-T
MyVariant Identifiers:
chrX:g.25004645G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25004645G>T , CM000685.2:g.25004645G>T | GRCh38 |
| NC_000023.10:g.25022762G>T , CM000685.1:g.25022762G>T | GRCh37 |
| NC_000023.9:g.24932683G>T | NCBI36 |
| NG_008281.1:g.16304C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.*25C>A MANE Select | ENSP00000368332.4:n.*25C>A | |
| ENST00000379044.4:c.*25C>A | ENSP00000368332.4:n.*25C>A | |
| NM_139058.2:c.*25C>A | NP_620689.1:n.*25C>A | |
| NM_139058.3:c.*25C>A MANE Select | NP_620689.1:n.*25C>A |