Linked Data
dbSNP Id:
rs782446763
ExAC:
X:154133113 G / A
gnomAD v2:
X-154133113-G-A
gnomAD v4:
X-154904838-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154904838G>A , CM000685.2:g.154904838G>A | GRCh38 |
| NC_000023.10:g.154133113G>A , CM000685.1:g.154133113G>A | GRCh37 |
| NC_000023.9:g.153786307G>A | NCBI36 |
| NG_011403.1:g.122886C>T | |
| NG_011403.2:g.122886C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5559C>T MANE Select | ENSP00000353393.4:p.Ala1853= | |
| ENST00000360256.8:c.5559C>T | ENSP00000353393.4:p.Ala1853= | |
| NM_000132.3:c.5559C>T | NP_000123.1:p.Ala1853= | |
| XM_011531126.1:c.5454C>T | XP_011529428.1:p.Ala1818= | |
| NM_000132.4:c.5559C>T MANE Select | NP_000123.1:p.Ala1853= |