Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52488371C>A , CM000674.2:g.52488371C>A | GRCh38 |
| NC_000012.11:g.52882155C>A , CM000674.1:g.52882155C>A | GRCh37 |
| NC_000012.10:g.51168422C>A | NCBI36 |
| NG_008298.1:g.10027G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005554.4:c.1381G>T MANE Select | NP_005545.1:p.Glu461Ter |
| ENST00000330722.7:c.1381G>T MANE Select | ENSP00000369317.3:p.Glu461Ter |
| NM_005554.3:c.1381G>T | NP_005545.1:p.Glu461Ter |
| ENST00000330722.6:c.1381G>T | ENSP00000369317.3:p.Glu461Ter |