Linked Data
dbSNP Id:
rs745468265
ExAC:
X:138642991 G / A
gnomAD v2:
X-138642991-G-A
gnomAD v3:
X-139560832-G-A
gnomAD v4:
X-139560832-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139560832G>A , CM000685.2:g.139560832G>A | GRCh38 |
| NC_000023.10:g.138642991G>A , CM000685.1:g.138642991G>A | GRCh37 |
| NC_000023.9:g.138470657G>A | NCBI36 |
| NG_007994.1:g.35097G>A , LRG_556:g.35097G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.815G>A MANE Select | ENSP00000218099.2:p.Gly272Asp | |
| ENST00000643157.1:n.1482G>A | ||
| ENST00000218099.6:c.815G>A | ENSP00000218099.2:p.Gly272Asp | |
| ENST00000394090.2:c.701G>A | ENSP00000377650.2:p.Gly234Asp | |
| NM_000133.3:c.815G>A , LRG_556t1:c.815G>A | NP_000124.1:p.Gly272Asp | |
| NM_001313913.1:c.701G>A | NP_001300842.1:p.Gly234Asp | |
| XM_005262397.3:c.686G>A | XP_005262454.1:p.Gly229Asp | |
| XM_005262397.4:c.686G>A | XP_005262454.1:p.Gly229Asp | |
| NM_000133.4:c.815G>A MANE Select | NP_000124.1:p.Gly272Asp | |
| NM_001313913.2:c.701G>A | NP_001300842.1:p.Gly234Asp |