Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186095484T= , CM000663.2:g.186095484T= | GRCh38 |
| NC_000001.10:g.186064616T= , CM000663.1:g.186064616T= | GRCh37 |
| NC_000001.9:g.184331239T= | NCBI36 |
| NG_011841.1:g.365934T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.10536T= MANE Select | ENSP00000271588.4:p.Ala3512= | |
| ENST00000271588.8:c.10536T= | ENSP00000271588.4:p.Ala3512= | |
| NM_031935.2:c.10536T= | NP_114141.2:p.Ala3512= | |
| XM_011510037.1:c.10251T= | XP_011508339.1:p.Ala3417= | |
| XM_011510038.1:c.10536T= | XP_011508340.1:p.Ala3512= | |
| XM_011510039.1:c.10536T= | XP_011508341.1:p.Ala3512= | |
| XM_011510038.3:c.10536T= | XP_011508340.1:p.Ala3512= | |
| XM_017002437.1:c.8559T= | XP_016857926.1:p.Ala2853= | |
| NM_031935.3:c.10536T= MANE Select | NP_114141.2:p.Ala3512= |