HGVS | Genome Assembly |
---|---|
NC_000005.10:g.45462204A>G , CM000667.2:g.45462204A>G | GRCh38 |
NC_000005.9:g.45462306A>G , CM000667.1:g.45462306A>G | GRCh37 |
NC_000005.8:g.45498063A>G | NCBI36 |
NG_042183.1:g.238915T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303230.6:c.850-197T>C MANE Select | ENSP00000307342.4:n.850-197T>C | |
ENST00000637305.1:n.13-197T>C | ||
ENST00000673735.1:c.850-197T>C | ENSP00000501107.1:n.850-197T>C | |
ENST00000303230.5:c.850-197T>C | ENSP00000307342.4:n.850-197T>C | |
NM_021072.3:c.850-197T>C | NP_066550.2:n.850-197T>C | |
NM_021072.4:c.850-197T>C MANE Select | NP_066550.2:n.850-197T>C |