Linked Data
ClinVar Variation Id:
1996068
ClinVar RCV Id:
RCV002801776
gnomAD v4:
X-25004886-C-G
MyVariant Identifiers:
chrX:g.25023003C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25004886C>G , CM000685.2:g.25004886C>G | GRCh38 |
| NC_000023.10:g.25023003C>G , CM000685.1:g.25023003C>G | GRCh37 |
| NC_000023.9:g.24932924C>G | NCBI36 |
| NG_008281.1:g.16063G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.1473G>C MANE Select | ENSP00000368332.4:p.Leu491= | |
| ENST00000636885.1:n.61G>C | ||
| ENST00000379044.4:c.1473G>C | ENSP00000368332.4:p.Leu491= | |
| NM_139058.2:c.1473G>C | NP_620689.1:p.Leu491= | |
| NM_139058.3:c.1473G>C MANE Select | NP_620689.1:p.Leu491= |