HGVS | Genome Assembly |
---|---|
NC_000011.10:g.44275637T>A , CM000673.2:g.44275637T>A | GRCh38 |
NC_000011.9:g.44297187T>A , CM000673.1:g.44297187T>A | GRCh37 |
NC_000011.8:g.44253763T>A | NCBI36 |
NG_015809.1:g.39530A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000652299.1:c.488A>T MANE Select | ENSP00000498217.1:p.Glu163Val | |
ENST00000329255.3:c.488A>T | ENSP00000332744.3:p.Glu163Val | |
NM_021926.3:c.488A>T | NP_068745.2:p.Glu163Val | |
XM_011520264.1:c.488A>T | XP_011518566.1:p.Glu163Val | |
XM_011520265.1:c.-35A>T | XP_011518567.1:n.-35A>T | |
XM_011520266.1:c.-35A>T | XP_011518568.1:n.-35A>T | |
NM_021926.4:c.488A>T MANE Select | NP_068745.2:p.Glu163Val |