Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128891379A= , CM000673.2:g.128891379A= | GRCh38 |
| NC_000011.9:g.128761274A= , CM000673.1:g.128761274A= | GRCh37 |
| NC_000011.8:g.128266484A= | NCBI36 |
| NG_023406.2:g.4962A= , LRG_333:g.4962A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529694.6:c.-353A= MANE Select | ENSP00000433295.1:n.-353A= | |
| ENST00000529694.5:c.-353A= | ENSP00000433295.1:n.-353A= | |
| NM_000890.4:c.-353A= | NP_000881.3:n.-353A= | |
| NM_001354169.1:c.-442A= | NP_001341098.1:n.-442A= | |
| NM_000890.5:c.-353A= MANE Select | NP_000881.3:n.-353A= | |
| NM_001354169.2:c.-442A= | NP_001341098.1:n.-442A= |