Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129818895C>T , CM000671.2:g.129818895C>T | GRCh38 |
| NC_000009.11:g.132581174C>T , CM000671.1:g.132581174C>T | GRCh37 |
| NC_000009.10:g.131620995C>T | NCBI36 |
| NG_008049.1:g.10268G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.470G>A MANE Select | ENSP00000345719.4:p.Gly157Asp | |
| ENST00000651202.1:c.566G>A | ENSP00000498222.1:p.Gly189Asp | |
| ENST00000351698.4:c.470G>A | ENSP00000345719.4:p.Gly157Asp | |
| ENST00000473604.2:n.580G>A | ||
| NM_000113.2:c.470G>A | NP_000104.1:p.Gly157Asp | |
| XR_929731.1:n.630G>A | ||
| XR_929731.3:n.498G>A | ||
| NM_000113.3:c.470G>A MANE Select | NP_000104.1:p.Gly157Asp |