Linked Data
dbSNP Id:
rs1306475866
gnomAD v3:
X-154191651-C-A
gnomAD v4:
X-154191651-C-A
MyVariant Identifiers:
chrX:g.154191651C>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154191651C>A , CM000685.2:g.154191651C>A | GRCh38 |
| NC_000023.10:g.153457142C>A , CM000685.1:g.153457142C>A | GRCh37 |
| NG_011606.1:g.14058C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000595290.6:c.579-37C>A MANE Select | ENSP00000472316.1:n.579-37C>A | |
| ENST00000595290.5:c.579-37C>A | ENSP00000472316.1:n.579-37C>A | |
| ENST00000595330.1:n.588+1429C>A | ||
| ENST00000596998.2:c.166-37C>A | ||
| NM_000513.2:c.579-37C>A MANE Select | NP_000504.1:n.579-37C>A |