Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6640620C>T , CM000673.2:g.6640620C>T | GRCh38 |
| NC_000011.9:g.6661851C>T , CM000673.1:g.6661851C>T | GRCh37 |
| NC_000011.8:g.6618427C>T | NCBI36 |
| NG_033858.1:g.20230G>A | |
| NG_033858.2:g.20230G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003737.4:c.994G>A MANE Select | NP_003728.1:p.Val332Met |
| ENST00000299441.5:c.994G>A MANE Select | ENSP00000299441.3:p.Val332Met |
| NM_003737.3:c.994G>A | NP_003728.1:p.Val332Met |
| ENST00000299441.4:c.994G>A | ENSP00000299441.3:p.Val332Met |