Linked Data
dbSNP Id:
rs1234142556
gnomAD v3:
X-154191672-C-T
gnomAD v4:
X-154191672-C-T
MyVariant Identifiers:
chrX:g.154191672C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154191672C>T , CM000685.2:g.154191672C>T | GRCh38 |
| NC_000023.10:g.153457163C>T , CM000685.1:g.153457163C>T | GRCh37 |
| NG_011606.1:g.14079C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000595290.6:c.579-16C>T MANE Select | ENSP00000472316.1:n.579-16C>T | |
| ENST00000595290.5:c.579-16C>T | ENSP00000472316.1:n.579-16C>T | |
| ENST00000595330.1:n.588+1450C>T | ||
| ENST00000596998.2:c.166-16C>T | ||
| NM_000513.2:c.579-16C>T MANE Select | NP_000504.1:n.579-16C>T |