Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186122957C= , CM000663.2:g.186122957C= | GRCh38 |
| NC_000001.10:g.186092089C= , CM000663.1:g.186092089C= | GRCh37 |
| NC_000001.9:g.184358712C= | NCBI36 |
| NG_011841.1:g.393407C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.12236C= MANE Select | ENSP00000271588.4:p.Pro4079= | |
| ENST00000271588.8:c.12236C= | ENSP00000271588.4:p.Pro4079= | |
| NM_031935.2:c.12236C= | NP_114141.2:p.Pro4079= | |
| XM_011510037.1:c.11951C= | XP_011508339.1:p.Pro3984= | |
| XM_011510038.1:c.12236C= | XP_011508340.1:p.Pro4079= | |
| XM_011510039.1:c.12236C= | XP_011508341.1:p.Pro4079= | |
| XM_011510038.3:c.12236C= | XP_011508340.1:p.Pro4079= | |
| XM_017002437.1:c.10259C= | XP_016857926.1:p.Pro3420= | |
| NM_031935.3:c.12236C= MANE Select | NP_114141.2:p.Pro4079= |