Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.21595867G>T , CM000668.2:g.21595867G>T | GRCh38 |
| NC_000006.11:g.21596098G>T , CM000668.1:g.21596098G>T | GRCh37 |
| NC_000006.10:g.21704077G>T | NCBI36 |
| NG_029166.1:g.7127G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003107.3:c.1333G>T MANE Select | NP_003098.1:p.Glu445Ter |
| ENST00000244745.4:c.1333G>T MANE Select | ENSP00000244745.1:p.Glu445Ter |
| NM_003107.2:c.1333G>T | NP_003098.1:p.Glu445Ter |
| ENST00000244745.2:c.1333G>T | ENSP00000244745.1:p.Glu445Ter |