Linked Data
dbSNP Id:
rs1557203797
gnomAD v2:
X-49957288-C-T
gnomAD v3:
X-50192637-C-T
gnomAD v4:
X-50192637-C-T
COSMIC:
COSM168722
MyVariant Identifiers:
chrX:g.49957288C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50192637C>T , CM000685.2:g.50192637C>T | GRCh38 |
| NC_000023.10:g.49957288C>T , CM000685.1:g.49957288C>T | GRCh37 |
| NC_000023.9:g.49844028C>T | NCBI36 |
| NG_012552.1:g.13377G>A | |
| NG_012552.2:g.13377G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358526.7:c.2076G>A MANE Select | ENSP00000351327.2:p.Ala692= | |
| ENST00000358526.6:c.2076G>A | ENSP00000351327.2:p.Ala692= | |
| ENST00000376064.7:c.2049G>A | ENSP00000365232.3:p.Ala683= | |
| ENST00000481402.5:n.2188G>A | ||
| NM_003886.2:c.2076G>A | NP_003877.2:p.Ala692= | |
| NM_139289.1:c.2049G>A | NP_647450.1:p.Ala683= | |
| NM_003886.3:c.2076G>A MANE Select | NP_003877.2:p.Ala692= | |
| NM_139289.2:c.2049G>A | NP_647450.1:p.Ala683= |