Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.45084778C>A , CM000669.2:g.45084778C>A | GRCh38 |
| NC_000007.13:g.45124377C>A , CM000669.1:g.45124377C>A | GRCh37 |
| NC_000007.12:g.45090902C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001146334.2:c.1402G>T MANE Select | NP_001139806.1:p.Val468Leu |
| ENST00000490531.3:c.1402G>T MANE Select | ENSP00000420477.2:p.Val468Leu |
| NM_001146334.1:c.1402G>T | NP_001139806.1:p.Val468Leu |
| ENST00000490531.2:c.1402G>T | ENSP00000420477.2:p.Val468Leu |
| XM_006715674.2:c.1402G>T | XP_006715737.1:p.Val468Leu |
| XM_006715674.3:c.1402G>T | XP_006715737.1:p.Val468Leu |
| XR_002956415.1:n.1960G>T |