Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24952656A= , CM000670.2:g.24952656A= | GRCh38 |
| NC_000008.10:g.24810169A= , CM000670.1:g.24810169A= | GRCh37 |
| NC_000008.9:g.24866086A= | NCBI36 |
| NG_008492.1:g.8962T= , LRG_259:g.8962T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610854.2:c.*154T= MANE Select | ENSP00000482169.2:n.*154T= | |
| ENST00000610854.1:c.*154T= | ENSP00000482169.1:n.*154T= | |
| ENST00000619417.1:c.*651T= | ENSP00000483690.1:n.*651T= | |
| NM_006158.4:c.*154T= , LRG_259t1:c.*154T= | NP_006149.2:n.*154T= | |
| NM_006158.5:c.*154T= MANE Select | NP_006149.2:n.*154T= |