Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154169C>T , CM000681.2:g.55154169C>T | GRCh38 |
| NC_000019.9:g.55665537C>T , CM000681.1:g.55665537C>T | GRCh37 |
| NC_000019.8:g.60357349C>T | NCBI36 |
| NG_007866.2:g.8564G>A , LRG_432:g.8564G>A | |
| NG_011829.2:g.70G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.410G>A MANE Select | ENSP00000341838.5:p.Gly137Asp | |
| ENST00000665070.1:c.443G>A | ENSP00000499482.1:p.Gly148Asp | |
| ENST00000344887.9:c.410G>A | ENSP00000341838.5:p.Gly137Asp | |
| ENST00000585806.5:n.409G>A | ||
| ENST00000586669.5:n.418G>A | ||
| ENST00000588882.1:c.335G>A | ENSP00000466729.1:p.Gly112Asp | |
| ENST00000589864.1:n.238G>A | ||
| NM_000363.4:c.410G>A , LRG_432t1:c.410G>A | NP_000354.4:p.Gly137Asp | |
| NM_000363.5:c.410G>A MANE Select | NP_000354.4:p.Gly137Asp |