Linked Data
dbSNP Id:
rs1032356229
gnomAD v3:
X-154904668-G-A
gnomAD v4:
X-154904668-G-A
MyVariant Identifiers:
chrX:g.154904668G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154904668G>A , CM000685.2:g.154904668G>A | GRCh38 |
| NC_000023.10:g.154132943G>A , CM000685.1:g.154132943G>A | GRCh37 |
| NC_000023.9:g.153786137G>A | NCBI36 |
| NG_011403.1:g.123056C>T | |
| NG_011403.2:g.123056C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5587-144C>T MANE Select | ENSP00000353393.4:n.5587-144C>T | |
| ENST00000360256.8:c.5587-144C>T | ENSP00000353393.4:n.5587-144C>T | |
| NM_000132.3:c.5587-144C>T | NP_000123.1:n.5587-144C>T | |
| XM_011531126.1:c.5482-144C>T | XP_011529428.1:n.5482-144C>T | |
| NM_000132.4:c.5587-144C>T MANE Select | NP_000123.1:n.5587-144C>T |