Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94421009G>C , CM000669.2:g.94421009G>C | GRCh38 |
| NC_000007.13:g.94050321G>C , CM000669.1:g.94050321G>C | GRCh37 |
| NC_000007.12:g.93888257G>C | NCBI36 |
| NG_007405.1:g.31449G>C , LRG_2:g.31449G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.2296G>C MANE Select | NP_000080.2:p.Gly766Arg |
| ENST00000297268.11:c.2296G>C MANE Select | ENSP00000297268.6:p.Gly766Arg |
| NM_000089.3:c.2296G>C , LRG_2t1:c.2296G>C | NP_000080.2:p.Gly766Arg |
| ENST00000297268.10:c.2296G>C | ENSP00000297268.6:p.Gly766Arg |
| ENST00000461525.5:n.385G>C | |
| ENST00000467931.1:n.676G>C | |
| ENST00000473573.5:n.633G>C | |
| ENST00000497316.5:n.693G>C | |
| ENST00000620463.1:c.2290G>C | ENSP00000477719.1:p.Gly764Arg |