Linked Data
dbSNP Id:
rs957046558
gnomAD v4:
X-48527070-G-A
MyVariant Identifiers:
chrX:g.48527070G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48527070G>A , CM000685.2:g.48527070G>A | GRCh38 |
| NC_000023.10:g.48385458G>A , CM000685.1:g.48385458G>A | GRCh37 |
| NC_000023.9:g.48270402G>A | NCBI36 |
| NG_007452.1:g.10295G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000495186.6:c.338+45G>A MANE Select | ENSP00000417052.1:n.338+45G>A | |
| ENST00000651615.1:c.338+45G>A | ENSP00000498524.1:n.338+45G>A | |
| ENST00000276096.10:n.296+45G>A | ||
| ENST00000414061.1:c.338+45G>A | ENSP00000405832.1:n.338+45G>A | |
| ENST00000446158.5:c.338+45G>A | ENSP00000390031.1:n.338+45G>A | |
| ENST00000466461.1:n.177+45G>A | ||
| ENST00000495186.5:c.338+45G>A | ENSP00000417052.1:n.338+45G>A | |
| ENST00000498425.1:n.459+45G>A | ||
| NM_006579.2:c.338+45G>A | NP_006570.1:n.338+45G>A | |
| NM_006579.3:c.338+45G>A MANE Select | NP_006570.1:n.338+45G>A |