Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81670861C= , CM000665.2:g.81670861C= | GRCh38 |
| NC_000003.11:g.81720012C= , CM000665.1:g.81720012C= | GRCh37 |
| NC_000003.10:g.81802702C= | NCBI36 |
| NG_011810.1:g.95940G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.406G= MANE Select | ENSP00000410833.2:p.Val136= | |
| ENST00000429644.6:c.406G= | ENSP00000410833.2:p.Val136= | |
| ENST00000477426.1:n.122G= | ||
| ENST00000489715.1:c.283G= | ENSP00000419638.1:p.Val95= | |
| NM_000158.3:c.406G= | NP_000149.3:p.Val136= | |
| NM_000158.4:c.406G= MANE Select | NP_000149.4:p.Val136= |