Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32445032T= , CM000668.2:g.32445032T= | GRCh38 |
| NC_000006.11:g.32412809T= , CM000668.1:g.32412809T= | GRCh37 |
| NC_000006.10:g.32520787T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019111.5:c.*392T= MANE Select | NP_061984.2:n.*392T= |
| ENST00000395388.7:c.*392T= MANE Select | ENSP00000378786.2:n.*392T= |
| NM_019111.4:c.*392T= | NP_061984.2:n.*392T= |
| ENST00000374982.5:c.*392T= | ENSP00000364121.5:n.*392T= |
| ENST00000395388.6:c.*392T= | ENSP00000378786.2:n.*392T= |