Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151526750A>G , CM000668.2:g.151526750A>G | GRCh38 |
| NC_000006.11:g.151847885A>G , CM000668.1:g.151847885A>G | GRCh37 |
| NC_000006.10:g.151889578A>G | NCBI36 |
| NG_021198.1:g.37711A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000239374.8:c.58-9568A>G MANE Select | ENSP00000239374.6:n.58-9568A>G | |
| ENST00000239374.7:c.58-9568A>G | ENSP00000239374.6:n.58-9568A>G | |
| NM_025059.3:c.58-9568A>G | NP_079335.2:n.58-9568A>G | |
| NM_025059.4:c.58-9568A>G MANE Select | NP_079335.2:n.58-9568A>G |