HGVS | Genome Assembly |
---|---|
NC_000005.10:g.45645220A= , CM000667.2:g.45645220A= | GRCh38 |
NC_000005.9:g.45645322A= , CM000667.1:g.45645322A= | GRCh37 |
NC_000005.8:g.45681079A= | NCBI36 |
NG_042183.1:g.55899T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303230.6:c.814T= MANE Select | ENSP00000307342.4:p.Ser272= | |
ENST00000637256.1:n.42T= | ||
ENST00000673735.1:c.814T= | ENSP00000501107.1:p.Ser272= | |
ENST00000303230.5:c.814T= | ENSP00000307342.4:p.Ser272= | |
ENST00000634658.1:c.814T= | ENSP00000489134.1:p.Ser272= | |
NM_021072.3:c.814T= | NP_066550.2:p.Ser272= | |
NM_021072.4:c.814T= MANE Select | NP_066550.2:p.Ser272= |