Linked Data
ClinVar Variation Id:
2996273
ClinVar RCV Id:
RCV003856424
gnomAD v4:
X-153725812-G-A
MyVariant Identifiers:
chrX:g.152991267G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153725812G>A , CM000685.2:g.153725812G>A | GRCh38 |
| NC_000023.10:g.152991267G>A , CM000685.1:g.152991267G>A | GRCh37 |
| NC_000023.9:g.152644461G>A | NCBI36 |
| NG_009022.2:g.5945G>A | |
| NG_023231.1:g.3935C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.546G>A MANE Select | ENSP00000218104.3:p.Arg182= | |
| ENST00000218104.5:c.546G>A | ENSP00000218104.3:p.Arg182= | |
| NM_000033.3:c.546G>A | NP_000024.2:p.Arg182= | |
| XR_938507.1:n.962G>A | ||
| XR_938507.2:n.962G>A | ||
| NM_000033.4:c.546G>A MANE Select | NP_000024.2:p.Arg182= |