Linked Data
dbSNP Id:
rs1162284802
gnomAD v3:
X-153742937-C-T
gnomAD v4:
X-153742937-C-T
MyVariant Identifiers:
chrX:g.153742937C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153742937C>T , CM000685.2:g.153742937C>T | GRCh38 |
| NC_000023.10:g.153008391C>T , CM000685.1:g.153008391C>T | GRCh37 |
| NC_000023.9:g.152661585C>T | NCBI36 |
| NG_009022.2:g.23070C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1781-50C>T MANE Select | ENSP00000218104.3:n.1781-50C>T | |
| ENST00000218104.5:c.1781-50C>T | ENSP00000218104.3:n.1781-50C>T | |
| NM_000033.3:c.1781-50C>T | NP_000024.2:n.1781-50C>T | |
| XR_938507.1:n.2253-50C>T | ||
| XR_938507.2:n.2253-50C>T | ||
| NM_000033.4:c.1781-50C>T MANE Select | NP_000024.2:n.1781-50C>T |