Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15440391G>A , CM000663.2:g.15440391G>A | GRCh38 |
| NC_000001.10:g.15766887G>A , CM000663.1:g.15766887G>A | GRCh37 |
| NC_000001.9:g.15639474G>A | NCBI36 |
| NG_009253.1:g.6950G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_007272.3:c.132G>A MANE Select | NP_009203.2:p.Gln44= |
| ENST00000375949.5:c.132G>A MANE Select | ENSP00000365116.4:p.Gln44= |
| NM_007272.2:c.132G>A | NP_009203.2:p.Gln44= |
| ENST00000375943.6:c.40+1887G>A | ENSP00000365110.2:n.40+1887G>A |
| ENST00000375949.4:c.132G>A | ENSP00000365116.4:p.Gln44= |
| ENST00000476813.5:n.52+1887G>A | |
| ENST00000483406.1:n.42G>A | |
| XM_011540550.1:c.132G>A | XP_011538852.1:p.Gln44= |