Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63972182C>T , CM000679.2:g.63972182C>T | GRCh38 |
| NC_000017.10:g.62049542C>T , CM000679.1:g.62049542C>T | GRCh37 |
| NC_000017.9:g.59403274C>T | NCBI36 |
| NG_011699.1:g.5737G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000334.4:c.436G>A MANE Select | NP_000325.4:p.Val146Ile |
| ENST00000435607.3:c.436G>A MANE Select | ENSP00000396320.1:p.Val146Ile |
| ENST00000578147.5:c.436G>A | ENSP00000463963.1:p.Val146Ile |
| XM_005257566.3:c.436G>A | XP_005257623.1:p.Val146Ile |