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