Linked Data
dbSNP Id:
rs1476125142
gnomAD v3:
X-53382152-T-A
gnomAD v4:
X-53382152-T-A
MyVariant Identifiers:
chrX:g.53382152T>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.53382152T>A , CM000685.2:g.53382152T>A | GRCh38 |
| NC_000023.10:g.53409073T>A , CM000685.1:g.53409073T>A | GRCh37 |
| NC_000023.9:g.53425798T>A | NCBI36 |
| NG_006988.2:g.45519A>T , LRG_773:g.45519A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322213.9:c.3437+80A>T MANE Select | ENSP00000323421.3:n.3437+80A>T | |
| ENST00000674590.1:c.2669+80A>T | ENSP00000502626.1:n.2669+80A>T | |
| ENST00000675504.1:c.3371+80A>T | ENSP00000502524.1:n.3371+80A>T | |
| ENST00000322213.8:c.3437+80A>T | ENSP00000323421.3:n.3437+80A>T | |
| ENST00000375340.10:c.3371+80A>T | ENSP00000364489.7:n.3371+80A>T | |
| ENST00000469129.1:n.373A>T | ||
| ENST00000470241.2:c.727+80A>T | ||
| NM_001281463.1:c.3371+80A>T , LRG_773t1:c.3371+80A>T | NP_001268392.1:n.3371+80A>T | |
| NM_006306.3:c.3437+80A>T , LRG_773t2:c.3437+80A>T | NP_006297.2:n.3437+80A>T | |
| NM_006306.4:c.3437+80A>T MANE Select | NP_006297.2:n.3437+80A>T |