HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114679633G= , CM000663.2:g.114679633G= | GRCh38 |
NC_000001.10:g.115222254G= , CM000663.1:g.115222254G= | GRCh37 |
NC_000001.9:g.115023777G= | NCBI36 |
NG_008012.1:g.20923C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369538.4:c.831C= | ENSP00000358551.4:p.Asp277= | |
ENST00000520113.7:c.843C= MANE Select | ENSP00000430075.3:p.Asp281= | |
ENST00000637080.1:c.626C= | ENSP00000489753.1:n.626C= | |
ENST00000639077.1:n.508C= | ||
ENST00000369538.3:c.930C= | ENSP00000358551.3:p.Asp310= | |
ENST00000520113.6:c.942C= | ENSP00000430075.2:p.Asp314= | |
NM_000036.2:c.942C= | NP_000027.2:p.Asp314= | |
NM_001172626.1:c.930C= | NP_001166097.1:p.Asp310= | |
NM_000036.3:c.843C= MANE Select | NP_000027.3:p.Asp281= | |
NM_001172626.2:c.831C= | NP_001166097.2:p.Asp277= |