Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24952575T= , CM000670.2:g.24952575T= | GRCh38 |
| NC_000008.10:g.24810088T= , CM000670.1:g.24810088T= | GRCh37 |
| NC_000008.9:g.24866005T= | NCBI36 |
| NG_008492.1:g.9043A= , LRG_259:g.9043A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006158.5:c.*235A= MANE Select | NP_006149.2:n.*235A= |
| ENST00000610854.2:c.*235A= MANE Select | ENSP00000482169.2:n.*235A= |
| NM_006158.4:c.*235A= , LRG_259t1:c.*235A= | NP_006149.2:n.*235A= |
| ENST00000610854.1:c.*235A= | ENSP00000482169.1:n.*235A= |
| ENST00000619417.1:c.*732A= | ENSP00000483690.1:n.*732A= |