Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.147413435G>T , CM000665.2:g.147413435G>T | GRCh38 |
| NC_000003.11:g.147131222G>T , CM000665.1:g.147131222G>T | GRCh37 |
| NC_000003.10:g.148613912G>T | NCBI36 |
| NG_015886.1:g.9042G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282928.5:c.1228G>T MANE Select | ENSP00000282928.4:p.Val410Leu | |
| ENST00000282928.4:c.1228G>T | ENSP00000282928.4:p.Val410Leu | |
| ENST00000472523.1:n.521+19493G>T | ||
| ENST00000488404.5:c.294G>T | ||
| NM_003412.3:c.1228G>T | NP_003403.2:p.Val410Leu | |
| NM_003412.4:c.1228G>T MANE Select | NP_003403.2:p.Val410Leu |