Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814752G>A , CM000664.2:g.218814752G>A | GRCh38 |
| NC_000002.11:g.219679475G>A , CM000664.1:g.219679475G>A | GRCh37 |
| NC_000002.10:g.219387719G>A | NCBI36 |
| NG_007959.1:g.38004G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000784.4:c.1471G>A MANE Select | NP_000775.1:p.Ala491Thr |
| ENST00000258415.9:c.1471G>A MANE Select | ENSP00000258415.4:p.Ala491Thr |
| NM_000784.3:c.1471G>A | NP_000775.1:p.Ala491Thr |
| ENST00000258415.8:c.1471G>A | ENSP00000258415.4:p.Ala491Thr |
| ENST00000494263.5:n.2183G>A | |
| XM_017003488.2:c.1051G>A | XP_016858977.1:p.Ala351Thr |