HGVS | Genome Assembly |
---|---|
NC_000015.10:g.23644565C= , CM000677.2:g.23644565C= | GRCh38 |
NC_000015.9:g.23889712C= , CM000677.1:g.23889712C= | GRCh37 |
NC_000015.8:g.21440805C= | NCBI36 |
NG_016776.1:g.8282G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650528.1:c.3178G= MANE Select | ENSP00000497810.1:p.Asp1060= | |
ENST00000532292.2:c.3178G= | ENSP00000433433.2:p.Asp1060= | |
NM_019066.4:c.3178G= | NP_061939.3:p.Asp1060= | |
NM_019066.5:c.3178G= MANE Select | NP_061939.3:p.Asp1060= |