Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37805076G>A , CM000685.2:g.37805076G>A | GRCh38 |
| NC_000023.10:g.37664329G>A , CM000685.1:g.37664329G>A | GRCh37 |
| NC_000023.9:g.37549273G>A | NCBI36 |
| NG_009065.1:g.30060G>A , LRG_53:g.30060G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696170.1:c.*731G>A | ENSP00000512461.1:n.*731G>A | |
| ENST00000696171.1:c.1126G>A | ENSP00000512462.1:p.Gly376Arg | |
| ENST00000378588.5:c.1222G>A MANE Select | ENSP00000367851.4:p.Gly408Arg | |
| ENST00000378588.4:c.1222G>A | ENSP00000367851.4:p.Gly408Arg | |
| ENST00000465127.1:c.171+379076G>A | ENSP00000417050.1:n.171+379076G>A | |
| NM_000397.3:c.1222G>A , LRG_53t1:c.1222G>A | NP_000388.2:p.Gly408Arg | |
| XM_011543890.1:c.916G>A | XP_011542192.1:p.Gly306Arg | |
| NM_000397.4:c.1222G>A MANE Select | NP_000388.2:p.Gly408Arg |