Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94421046G>C , CM000669.2:g.94421046G>C | GRCh38 |
| NC_000007.13:g.94050358G>C , CM000669.1:g.94050358G>C | GRCh37 |
| NC_000007.12:g.93888294G>C | NCBI36 |
| NG_007405.1:g.31486G>C , LRG_2:g.31486G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.2333G>C MANE Select | NP_000080.2:p.Gly778Ala |
| ENST00000297268.11:c.2333G>C MANE Select | ENSP00000297268.6:p.Gly778Ala |
| NM_000089.3:c.2333G>C , LRG_2t1:c.2333G>C | NP_000080.2:p.Gly778Ala |
| ENST00000297268.10:c.2333G>C | ENSP00000297268.6:p.Gly778Ala |
| ENST00000461525.5:n.422G>C | |
| ENST00000467931.1:n.713G>C | |
| ENST00000473573.5:n.670G>C | |
| ENST00000497316.5:n.730G>C | |
| ENST00000620463.1:c.2327G>C | ENSP00000477719.1:p.Gly776Ala |