Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.21312444A>G , CM000676.2:g.21312444A>G | GRCh38 |
| NC_000014.8:g.21780603A>G , CM000676.1:g.21780603A>G | GRCh37 |
| NC_000014.7:g.20850443A>G | NCBI36 |
| NG_008933.1:g.29468A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400017.7:c.1089A>G MANE Select | ENSP00000382895.2:p.Arg363= | |
| ENST00000400017.6:c.1089A>G | ENSP00000382895.2:p.Arg363= | |
| ENST00000556336.5:c.1008A>G | ENSP00000450445.1:p.Arg336= | |
| ENST00000557771.5:c.1008A>G | ENSP00000451219.1:p.Arg336= | |
| NM_020366.3:c.1089A>G | NP_065099.3:p.Arg363= | |
| XM_011536983.1:c.1056A>G | XP_011535285.1:p.Arg352= | |
| NM_020366.4:c.1089A>G MANE Select | NP_065099.3:p.Arg363= |