HGVS | Genome Assembly |
---|---|
NC_000015.10:g.97960846A>G , CM000677.2:g.97960846A>G | GRCh38 |
NC_000015.9:g.98504076A>G , CM000677.1:g.98504076A>G | GRCh37 |
NC_000015.8:g.96305080A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000268042.7:c.-16A>G MANE Select | ENSP00000268042.6:n.-16A>G | |
ENST00000268042.6:c.-16A>G | ENSP00000268042.6:n.-16A>G | |
NM_183376.2:c.-16A>G | NP_899232.2:n.-16A>G | |
NM_183376.3:c.-16A>G MANE Select | NP_899232.2:n.-16A>G |