Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15443547G>A , CM000663.2:g.15443547G>A | GRCh38 |
| NC_000001.10:g.15770042G>A , CM000663.1:g.15770042G>A | GRCh37 |
| NC_000001.9:g.15642629G>A | NCBI36 |
| NG_009253.1:g.10105G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_007272.3:c.485G>A MANE Select | NP_009203.2:p.Arg162His |
| ENST00000375949.5:c.485G>A MANE Select | ENSP00000365116.4:p.Arg162His |
| NM_007272.2:c.485G>A | NP_009203.2:p.Arg162His |
| ENST00000375943.6:c.*85G>A | ENSP00000365110.2:n.*85G>A |
| ENST00000375949.4:c.485G>A | ENSP00000365116.4:p.Arg162His |
| ENST00000483406.1:n.395G>A | |
| XM_011540550.1:c.485G>A | XP_011538852.1:p.Arg162His |