HGVS | Genome Assembly |
---|---|
NC_000005.10:g.45645501A>G , CM000667.2:g.45645501A>G | GRCh38 |
NC_000005.9:g.45645603A>G , CM000667.1:g.45645603A>G | GRCh37 |
NC_000005.8:g.45681360A>G | NCBI36 |
NG_042183.1:g.55618T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000303230.6:c.533T>C MANE Select | ENSP00000307342.4:p.Phe178Ser | |
ENST00000673735.1:c.533T>C | ENSP00000501107.1:p.Phe178Ser | |
ENST00000303230.5:c.533T>C | ENSP00000307342.4:p.Phe178Ser | |
ENST00000634658.1:c.533T>C | ENSP00000489134.1:p.Phe178Ser | |
NM_021072.3:c.533T>C | NP_066550.2:p.Phe178Ser | |
NM_021072.4:c.533T>C MANE Select | NP_066550.2:p.Phe178Ser |