HGVS | Genome Assembly |
---|---|
NC_000005.10:g.141331048G= , CM000667.2:g.141331048G= | GRCh38 |
NC_000005.9:g.140710615G= , CM000667.1:g.140710615G= | GRCh37 |
NC_000005.8:g.140690799G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000517417.3:c.364G= MANE Select | ENSP00000431083.1:p.Glu122= | |
ENST00000378105.4:c.364G= | ENSP00000367345.3:p.Glu122= | |
ENST00000517417.2:c.364G= | ENSP00000431083.1:p.Glu122= | |
NM_018912.2:c.364G= | NP_061735.1:p.Glu122= | |
NM_031993.1:c.364G= | NP_114382.1:p.Glu122= | |
NM_018912.3:c.364G= MANE Select | NP_061735.1:p.Glu122= | |
NM_031993.2:c.364G= | NP_114382.1:p.Glu122= |