Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186166912C= , CM000663.2:g.186166912C= | GRCh38 |
| NC_000001.10:g.186136044C= , CM000663.1:g.186136044C= | GRCh37 |
| NC_000001.9:g.184402667C= | NCBI36 |
| NG_011841.1:g.437362C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.15544C= MANE Select | ENSP00000271588.4:p.Arg5182= | |
| ENST00000271588.8:c.15544C= | ENSP00000271588.4:p.Arg5182= | |
| ENST00000475585.1:n.163-4425C= | ||
| NM_031935.2:c.15544C= | NP_114141.2:p.Arg5182= | |
| XM_011510037.1:c.15259C= | XP_011508339.1:p.Arg5087= | |
| XM_011510038.1:c.15544C= | XP_011508340.1:p.Arg5182= | |
| XM_011510038.3:c.15544C= | XP_011508340.1:p.Arg5182= | |
| XM_017002437.1:c.13567C= | XP_016857926.1:p.Arg4523= | |
| NM_031935.3:c.15544C= MANE Select | NP_114141.2:p.Arg5182= |