HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3154717G>T , CM000668.2:g.3154717G>T | GRCh38 |
NC_000006.11:g.3154951G>T , CM000668.1:g.3154951G>T | GRCh37 |
NC_000006.10:g.3099950G>T | NCBI36 |
NG_042223.1:g.7833C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333628.4:c.484C>A MANE Select | ENSP00000369703.2:p.Arg162Ser | |
ENST00000679400.1:n.540C>A | ||
ENST00000679907.1:n.872C>A | ||
ENST00000680036.1:n.1266C>A | ||
ENST00000680967.1:n.1574C>A | ||
ENST00000333628.3:c.484C>A | ENSP00000369703.2:p.Arg162Ser | |
ENST00000489942.1:n.679C>A | ||
NM_001069.2:c.484C>A | NP_001060.1:p.Arg162Ser | |
NM_001310315.1:c.229C>A | NP_001297244.1:p.Arg77Ser | |
NM_001069.3:c.484C>A MANE Select | NP_001060.1:p.Arg162Ser | |
NM_001310315.2:c.229C>A | NP_001297244.1:p.Arg77Ser |