Linked Data
ClinVar Variation Id:
1092499
ClinVar RCV Id:
RCV001412361
dbSNP Id:
rs2147345156
gnomAD v4:
X-38408947-C-T
MyVariant Identifiers:
chrX:g.38268200C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38408947C>T , CM000685.2:g.38408947C>T | GRCh38 |
| NC_000023.10:g.38268200C>T , CM000685.1:g.38268200C>T | GRCh37 |
| NC_000023.9:g.38153144C>T | NCBI36 |
| NG_008471.1:g.61465C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.789C>T MANE Select | ENSP00000039007.4:p.Asp263= | |
| ENST00000643344.1:c.*539C>T | ENSP00000496606.1:n.*539C>T | |
| ENST00000039007.4:c.789C>T | ENSP00000039007.4:p.Asp263= | |
| ENST00000465127.1:c.172-257174C>T | ENSP00000417050.1:n.172-257174C>T | |
| NM_000531.5:c.789C>T | NP_000522.3:p.Asp263= | |
| XM_017029556.1:c.789C>T | XP_016885045.1:p.Asp263= | |
| NM_000531.6:c.789C>T MANE Select | NP_000522.3:p.Asp263= |