Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.44942213G>C , CM000664.2:g.44942213G>C | GRCh38 |
| NC_000002.11:g.45169352G>C , CM000664.1:g.45169352G>C | GRCh37 |
| NC_000002.10:g.45022856G>C | NCBI36 |
| NG_016222.1:g.5316G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260653.5:c.109G>C MANE Select | ENSP00000260653.3:p.Gly37Arg | |
| ENST00000260653.4:c.109G>C | ENSP00000260653.3:p.Gly37Arg | |
| NM_005413.3:c.109G>C | NP_005404.1:p.Gly37Arg | |
| XM_011533042.1:c.109G>C | XP_011531344.1:p.Gly37Arg | |
| NM_005413.4:c.109G>C MANE Select | NP_005404.1:p.Gly37Arg |