Linked Data
ClinVar Variation Id:
797517
ClinVar RCV Id:
RCV001396772
dbSNP Id:
rs1021002740
gnomAD v3:
X-25004868-C-A
gnomAD v4:
X-25004868-C-A
MyVariant Identifiers:
chrX:g.25022985C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25004868C>A , CM000685.2:g.25004868C>A | GRCh38 |
| NC_000023.10:g.25022985C>A , CM000685.1:g.25022985C>A | GRCh37 |
| NC_000023.9:g.24932906C>A | NCBI36 |
| NG_008281.1:g.16081G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.1491G>T MANE Select | ENSP00000368332.4:p.Ala497= | |
| ENST00000636885.1:n.79G>T | ||
| ENST00000379044.4:c.1491G>T | ENSP00000368332.4:p.Ala497= | |
| NM_139058.2:c.1491G>T | NP_620689.1:p.Ala497= | |
| NM_139058.3:c.1491G>T MANE Select | NP_620689.1:p.Ala497= |