Linked Data
dbSNP Id:
rs1557275617
gnomAD v2:
X-154124514-A-T
gnomAD v3:
X-154896239-A-T
gnomAD v4:
X-154896239-A-T
MyVariant Identifiers:
chrX:g.154124514A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154896239A>T , CM000685.2:g.154896239A>T | GRCh38 |
| NC_000023.10:g.154124514A>T , CM000685.1:g.154124514A>T | GRCh37 |
| NC_000023.9:g.153777708A>T | NCBI36 |
| NG_011403.1:g.131485T>A | |
| NG_011403.2:g.131485T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.6274-7T>A MANE Select | ENSP00000353393.4:n.6274-7T>A | |
| ENST00000360256.8:c.6274-7T>A | ENSP00000353393.4:n.6274-7T>A | |
| NM_000132.3:c.6274-7T>A | NP_000123.1:n.6274-7T>A | |
| XM_011531126.1:c.6169-7T>A | XP_011529428.1:n.6169-7T>A | |
| NM_000132.4:c.6274-7T>A MANE Select | NP_000123.1:n.6274-7T>A |