HGVS | Genome Assembly |
---|---|
NC_000005.10:g.45645545T>C , CM000667.2:g.45645545T>C | GRCh38 |
NC_000005.9:g.45645647T>C , CM000667.1:g.45645647T>C | GRCh37 |
NC_000005.8:g.45681404T>C | NCBI36 |
NG_042183.1:g.55574A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000303230.6:c.489A>G MANE Select | ENSP00000307342.4:p.Gly163= | |
ENST00000673735.1:c.489A>G | ENSP00000501107.1:p.Gly163= | |
ENST00000303230.5:c.489A>G | ENSP00000307342.4:p.Gly163= | |
ENST00000634658.1:c.489A>G | ENSP00000489134.1:p.Gly163= | |
NM_021072.3:c.489A>G | NP_066550.2:p.Gly163= | |
NM_021072.4:c.489A>G MANE Select | NP_066550.2:p.Gly163= |