Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29920614T>C , CM000664.2:g.29920614T>C | GRCh38 |
| NC_000002.11:g.30143480T>C , CM000664.1:g.30143480T>C | GRCh37 |
| NC_000002.10:g.29996984T>C | NCBI36 |
| NG_009445.1:g.5953A>G , LRG_488:g.5953A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004304.5:c.46A>G MANE Select | NP_004295.2:p.Thr16Ala |
| ENST00000389048.8:c.46A>G MANE Select | ENSP00000373700.3:p.Thr16Ala |
| NM_004304.4:c.46A>G | NP_004295.2:p.Thr16Ala |
| ENST00000389048.7:c.46A>G | ENSP00000373700.3:p.Thr16Ala |
| XR_001738688.2:n.976A>G |