HGVS | Genome Assembly |
---|---|
NC_000005.10:g.71719562G= , CM000667.2:g.71719562G= | GRCh38 |
NC_000005.9:g.71015389G= , CM000667.1:g.71015389G= | GRCh37 |
NC_000005.8:g.71051145G= | NCBI36 |
NG_015988.1:g.5400G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296777.5:c.159+110G= MANE Select | ENSP00000296777.4:n.159+110G= | |
ENST00000296777.4:c.159+110G= | ENSP00000296777.4:n.159+110G= | |
NM_004291.3:c.159+110G= | NP_004282.1:n.159+110G= | |
NM_004291.4:c.159+110G= MANE Select | NP_004282.1:n.159+110G= |