Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160242388T>A , CM000668.2:g.160242388T>A | GRCh38 |
| NC_000006.11:g.160663420T>A , CM000668.1:g.160663420T>A | GRCh37 |
| NC_000006.10:g.160583410T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003058.4:c.1294A>T MANE Select | NP_003049.2:p.Lys432Ter |
| ENST00000366953.8:c.1294A>T MANE Select | ENSP00000355920.3:p.Lys432Ter |
| NM_003058.3:c.1294A>T | NP_003049.2:p.Lys432Ter |
| ENST00000366953.7:c.1294A>T | ENSP00000355920.3:p.Lys432Ter |
| ENST00000486916.5:n.333A>T | |
| ENST00000491092.1:n.1191A>T |