Linked Data
dbSNP Id:
rs1557276237
gnomAD v2:
X-154133306-AC-A
gnomAD v4:
X-154905031-AC-A
MyVariant Identifiers:
chrX:g.154133307del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154905032del , CM000685.2:g.154905032del | GRCh38 |
| NC_000023.10:g.154133307del , CM000685.1:g.154133307del | GRCh37 |
| NC_000023.9:g.153786501del | NCBI36 |
| NG_011403.1:g.122692del | |
| NG_011403.2:g.122692del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5374-9del MANE Select | ENSP00000353393.4:n.5374-9del | |
| ENST00000360256.8:c.5374-9del | ENSP00000353393.4:n.5374-9del | |
| NM_000132.3:c.5374-9del | NP_000123.1:n.5374-9del | |
| XM_011531126.1:c.5269-9del | XP_011529428.1:n.5269-9del | |
| NM_000132.4:c.5374-9del MANE Select | NP_000123.1:n.5374-9del |