HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52652090C= , CM000674.2:g.52652090C= | GRCh38 |
NC_000012.11:g.53045874C= , CM000674.1:g.53045874C= | GRCh37 |
NC_000012.10:g.51332141C= | NCBI36 |
NG_008296.1:g.5086G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309680.4:c.53G= MANE Select | ENSP00000310861.3:p.Gly18= | |
ENST00000309680.3:c.53G= | ENSP00000310861.3:p.Gly18= | |
NM_000423.2:c.53G= | NP_000414.2:p.Gly18= | |
NM_000423.3:c.53G= MANE Select | NP_000414.2:p.Gly18= |