Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55151880T>C , CM000681.2:g.55151880T>C | GRCh38 |
| NC_000019.9:g.55663248T>C , CM000681.1:g.55663248T>C | GRCh37 |
| NC_000019.8:g.60355060T>C | NCBI36 |
| NG_007866.2:g.10853A>G , LRG_432:g.10853A>G | |
| NG_011829.2:g.2359A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.587A>G MANE Select | NP_000354.4:p.Asp196Gly |
| ENST00000344887.10:c.587A>G MANE Select | ENSP00000341838.5:p.Asp196Gly |
| NM_000363.4:c.587A>G , LRG_432t1:c.587A>G | NP_000354.4:p.Asp196Gly |
| ENST00000344887.9:c.587A>G | ENSP00000341838.5:p.Asp196Gly |
| ENST00000585806.5:n.586A>G | |
| ENST00000588882.1:c.512A>G | ENSP00000466729.1:p.Asp171Gly |
| ENST00000589864.1:n.415A>G | |
| ENST00000665070.1:c.620A>G | ENSP00000499482.1:p.Asp207Gly |