Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49124878T= , CM000665.2:g.49124878T= | GRCh38 |
| NC_000003.11:g.49162311T= , CM000665.1:g.49162311T= | GRCh37 |
| NC_000003.10:g.49137315T= | NCBI36 |
| NG_008094.1:g.13289A= | |
| NG_054716.1:g.1061A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305544.9:c.2932A= MANE Select | ENSP00000307156.4:p.Arg978= | |
| ENST00000305544.8:c.2932A= | ENSP00000307156.4:p.Arg978= | |
| ENST00000418109.5:c.2932A= | ENSP00000388325.1:p.Arg978= | |
| ENST00000462930.5:n.339A= | ||
| ENST00000464891.5:n.665A= | ||
| ENST00000483057.1:n.532A= | ||
| ENST00000542580.1:n.247A= | ||
| NM_002292.3:c.2932A= | NP_002283.3:p.Arg978= | |
| XM_005265127.3:c.2932A= | XP_005265184.1:p.Arg978= | |
| XM_005265127.4:c.2932A= | XP_005265184.1:p.Arg978= | |
| NM_002292.4:c.2932A= MANE Select | NP_002283.3:p.Arg978= |