Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.203183673T= , CM000663.2:g.203183673T= | GRCh38 |
| NC_000001.10:g.203152801T= , CM000663.1:g.203152801T= | GRCh37 |
| NC_000001.9:g.201419424T= | NCBI36 |
| NG_013056.1:g.8122A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001276.4:c.433A= MANE Select | NP_001267.2:p.Arg145= |
| ENST00000255409.8:c.433A= MANE Select | ENSP00000255409.3:p.Arg145= |
| NM_001276.2:c.433A= | NP_001267.2:p.Arg145= |
| NM_001276.3:c.433A= | NP_001267.2:p.Arg145= |
| ENST00000255409.7:c.433A= | ENSP00000255409.3:p.Arg145= |
| XM_011509105.1:c.451A= | XP_011507407.1:p.Arg151= |
| XM_011509106.1:c.451A= | XP_011507408.1:p.Arg151= |
| XM_011509107.1:c.433A= | XP_011507409.1:p.Arg145= |
| XM_011509108.1:c.451A= | XP_011507410.1:p.Arg151= |