Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232652C>A , CM000667.2:g.173232652C>A | GRCh38 |
| NC_000005.9:g.172659655C>A , CM000667.1:g.172659655C>A | GRCh37 |
| NC_000005.8:g.172592261C>A | NCBI36 |
| NG_013340.1:g.7661G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.892G>T MANE Select | ENSP00000327758.4:p.Gly298Trp | |
| ENST00000329198.4:c.892G>T | ENSP00000327758.4:p.Gly298Trp | |
| NM_001166175.1:c.*845G>T | NP_001159647.1:n.*845G>T | |
| NM_001166176.1:c.*691G>T | NP_001159648.1:n.*691G>T | |
| NM_004387.3:c.892G>T | NP_004378.1:p.Gly298Trp | |
| NM_004387.4:c.892G>T MANE Select | NP_004378.1:p.Gly298Trp | |
| NM_001166175.2:c.*845G>T | NP_001159647.1:n.*845G>T | |
| NM_001166176.2:c.*691G>T | NP_001159648.1:n.*691G>T |