Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186095488G= , CM000663.2:g.186095488G= | GRCh38 |
| NC_000001.10:g.186064620G= , CM000663.1:g.186064620G= | GRCh37 |
| NC_000001.9:g.184331243G= | NCBI36 |
| NG_011841.1:g.365938G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.10540G= MANE Select | ENSP00000271588.4:p.Glu3514= | |
| ENST00000271588.8:c.10540G= | ENSP00000271588.4:p.Glu3514= | |
| NM_031935.2:c.10540G= | NP_114141.2:p.Glu3514= | |
| XM_011510037.1:c.10255G= | XP_011508339.1:p.Glu3419= | |
| XM_011510038.1:c.10540G= | XP_011508340.1:p.Glu3514= | |
| XM_011510039.1:c.10540G= | XP_011508341.1:p.Glu3514= | |
| XM_011510038.3:c.10540G= | XP_011508340.1:p.Glu3514= | |
| XM_017002437.1:c.8563G= | XP_016857926.1:p.Glu2855= | |
| NM_031935.3:c.10540G= MANE Select | NP_114141.2:p.Glu3514= |