Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29228930C>T , CM000664.2:g.29228930C>T | GRCh38 |
| NC_000002.11:g.29451796C>T , CM000664.1:g.29451796C>T | GRCh37 |
| NC_000002.10:g.29305300C>T | NCBI36 |
| NG_009445.1:g.697637G>A , LRG_488:g.697637G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004304.5:c.2769G>A MANE Select | NP_004295.2:p.Gly923= |
| ENST00000389048.8:c.2769G>A MANE Select | ENSP00000373700.3:p.Gly923= |
| NM_004304.4:c.2769G>A | NP_004295.2:p.Gly923= |
| ENST00000389048.7:c.2769G>A | ENSP00000373700.3:p.Gly923= |
| ENST00000618119.4:c.1638G>A | ENSP00000482733.1:p.Gly546= |
| XM_024452778.1:c.-33+28G>A | XP_024308546.1:n.-33+28G>A |
| XR_001738688.2:n.3671+28G>A |