Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186166799C= , CM000663.2:g.186166799C= | GRCh38 |
| NC_000001.10:g.186135931C= , CM000663.1:g.186135931C= | GRCh37 |
| NC_000001.9:g.184402554C= | NCBI36 |
| NG_011841.1:g.437249C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.15440-9C= MANE Select | ENSP00000271588.4:n.15440-9C= | |
| ENST00000271588.8:c.15440-9C= | ENSP00000271588.4:n.15440-9C= | |
| ENST00000475585.1:n.163-4538C= | ||
| NM_031935.2:c.15440-9C= | NP_114141.2:n.15440-9C= | |
| XM_011510037.1:c.15155-9C= | XP_011508339.1:n.15155-9C= | |
| XM_011510038.1:c.15440-9C= | XP_011508340.1:n.15440-9C= | |
| XM_011510038.3:c.15440-9C= | XP_011508340.1:n.15440-9C= | |
| XM_017002437.1:c.13463-9C= | XP_016857926.1:n.13463-9C= | |
| NM_031935.3:c.15440-9C= MANE Select | NP_114141.2:n.15440-9C= |