Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186174533T= , CM000663.2:g.186174533T= | GRCh38 |
| NC_000001.10:g.186143665T= , CM000663.1:g.186143665T= | GRCh37 |
| NC_000001.9:g.184410288T= | NCBI36 |
| NG_011841.1:g.444983T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.15834T= MANE Select | ENSP00000271588.4:p.Asp5278= | |
| ENST00000271588.8:c.15834T= | ENSP00000271588.4:p.Asp5278= | |
| ENST00000414277.1:c.210T= | ENSP00000406205.1:p.Asp70= | |
| NM_031935.2:c.15834T= | NP_114141.2:p.Asp5278= | |
| XM_011510037.1:c.15549T= | XP_011508339.1:p.Asp5183= | |
| XM_011510038.1:c.15834T= | XP_011508340.1:p.Asp5278= | |
| XM_011510038.3:c.15834T= | XP_011508340.1:p.Asp5278= | |
| XM_017002437.1:c.13857T= | XP_016857926.1:p.Asp4619= | |
| NM_031935.3:c.15834T= MANE Select | NP_114141.2:p.Asp5278= |