Linked Data
MyVariant Identifiers:
chrX:g.153453518T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154188029T>A , CM000685.2:g.154188029T>A | GRCh38 |
| NC_000023.10:g.153453518T>A , CM000685.1:g.153453518T>A | GRCh37 |
| NG_011606.1:g.10434T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000595290.6:c.372T>A MANE Select | ENSP00000472316.1:p.Pro124= | |
| ENST00000595290.5:c.372T>A | ENSP00000472316.1:p.Pro124= | |
| ENST00000595330.1:n.382T>A | ||
| NM_000513.2:c.372T>A MANE Select | NP_000504.1:p.Pro124= |