Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186166804G= , CM000663.2:g.186166804G= | GRCh38 |
| NC_000001.10:g.186135936G= , CM000663.1:g.186135936G= | GRCh37 |
| NC_000001.9:g.184402559G= | NCBI36 |
| NG_011841.1:g.437254G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_031935.3:c.15440-4G= MANE Select | NP_114141.2:n.15440-4G= |
| ENST00000271588.9:c.15440-4G= MANE Select | ENSP00000271588.4:n.15440-4G= |
| NM_031935.2:c.15440-4G= | NP_114141.2:n.15440-4G= |
| ENST00000271588.8:c.15440-4G= | ENSP00000271588.4:n.15440-4G= |
| ENST00000475585.1:n.163-4533G= | |
| XM_011510037.1:c.15155-4G= | XP_011508339.1:n.15155-4G= |
| XM_011510038.1:c.15440-4G= | XP_011508340.1:n.15440-4G= |
| XM_011510038.3:c.15440-4G= | XP_011508340.1:n.15440-4G= |
| XM_017002437.1:c.13463-4G= | XP_016857926.1:n.13463-4G= |