Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.182585980G= , CM000663.2:g.182585980G= | GRCh38 |
| NC_000001.10:g.182555115G= , CM000663.1:g.182555115G= | GRCh37 |
| NC_000001.9:g.180821738G= | NCBI36 |
| NG_009024.2:g.5994C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021133.4:c.827C= MANE Select | NP_066956.1:p.Ala276= |
| ENST00000367559.7:c.827C= MANE Select | ENSP00000356530.3:p.Ala276= |
| NM_021133.3:c.827C= | NP_066956.1:p.Ala276= |
| ENST00000539397.1:c.827C= | ENSP00000440844.1:p.Ala276= |
| XM_005245411.2:c.827C= | XP_005245468.1:p.Ala276= |
| XR_001737359.1:n.1110C= | |
| XR_001737360.1:n.1110C= |