Linked Data
dbSNP Id:
rs1462376958
gnomAD v3:
X-154961042-T-A
gnomAD v4:
X-154961042-T-A
MyVariant Identifiers:
chrX:g.154961042T>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154961042T>A , CM000685.2:g.154961042T>A | GRCh38 |
| NC_000023.10:g.154189317T>A , CM000685.1:g.154189317T>A | GRCh37 |
| NC_000023.9:g.153842511T>A | NCBI36 |
| NG_011403.1:g.66682A>T | |
| NG_011403.2:g.66682A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.1537+33A>T MANE Select | ENSP00000353393.4:n.1537+33A>T | |
| ENST00000647125.1:c.*1413+33A>T | ENSP00000496062.1:n.*1413+33A>T | |
| ENST00000360256.8:c.1537+33A>T | ENSP00000353393.4:n.1537+33A>T | |
| NM_000132.3:c.1537+33A>T | NP_000123.1:n.1537+33A>T | |
| XM_011531126.1:c.1432+33A>T | XP_011529428.1:n.1432+33A>T | |
| NM_000132.4:c.1537+33A>T MANE Select | NP_000123.1:n.1537+33A>T |