Linked Data
dbSNP Id:
rs1557054188
gnomAD v2:
X-153001721-C-T
gnomAD v4:
X-153736267-C-T
MyVariant Identifiers:
chrX:g.153001721C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153736267C>T , CM000685.2:g.153736267C>T | GRCh38 |
| NC_000023.10:g.153001721C>T , CM000685.1:g.153001721C>T | GRCh37 |
| NC_000023.9:g.152654915C>T | NCBI36 |
| NG_009022.2:g.16400C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1224+13C>T MANE Select | ENSP00000218104.3:n.1224+13C>T | |
| ENST00000218104.5:c.1224+13C>T | ENSP00000218104.3:n.1224+13C>T | |
| ENST00000443684.2:n.227+13C>T | ||
| NM_000033.3:c.1224+13C>T | NP_000024.2:n.1224+13C>T | |
| XR_938507.1:n.1640+13C>T | ||
| XR_938507.2:n.1640+13C>T | ||
| NM_000033.4:c.1224+13C>T MANE Select | NP_000024.2:n.1224+13C>T |