HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52651995C>T , CM000674.2:g.52651995C>T | GRCh38 |
NC_000012.11:g.53045779C>T , CM000674.1:g.53045779C>T | GRCh37 |
NC_000012.10:g.51332046C>T | NCBI36 |
NG_008296.1:g.5181G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309680.4:c.148G>A MANE Select | ENSP00000310861.3:p.Gly50Ser | |
ENST00000309680.3:c.148G>A | ENSP00000310861.3:p.Gly50Ser | |
NM_000423.2:c.148G>A | NP_000414.2:p.Gly50Ser | |
NM_000423.3:c.148G>A MANE Select | NP_000414.2:p.Gly50Ser |