Linked Data
ClinVar Variation Id:
1741554
ClinVar RCV Id:
RCV002342121
gnomAD v4:
X-74421871-G-A
MyVariant Identifiers:
chrX:g.73641706G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.74421871G>A , CM000685.2:g.74421871G>A | GRCh38 |
| NC_000023.10:g.73641706G>A , CM000685.1:g.73641706G>A | GRCh37 |
| NC_000023.9:g.73558431G>A | NCBI36 |
| NG_011641.1:g.5622G>A | |
| NG_011641.2:g.5622G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000587091.6:c.234G>A MANE Select | ENSP00000465734.1:p.Glu78= | |
| ENST00000587091.5:c.234G>A | ENSP00000465734.1:p.Glu78= | |
| NM_006517.4:c.234G>A | NP_006508.2:p.Glu78= | |
| XM_005262294.1:c.234G>A | XP_005262351.1:p.Glu78= | |
| XM_011531015.1:c.234G>A | XP_011529317.1:p.Glu78= | |
| NM_006517.5:c.234G>A MANE Select | NP_006508.2:p.Glu78= |