HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320459C= , CM000667.2:g.159320459C= | GRCh38 |
NC_000005.9:g.158747467C= , CM000667.1:g.158747467C= | GRCh37 |
NC_000005.8:g.158680045C= | NCBI36 |
NG_009618.1:g.15015G= , LRG_71:g.15015G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.-87G= | ENSP00000512849.1:n.-87G= | |
ENST00000696751.1:c.*39G= | ENSP00000512850.1:n.*39G= | |
ENST00000231228.3:c.544G= MANE Select | ENSP00000231228.2:p.Gly182= | |
ENST00000231228.2:c.544G= | ENSP00000231228.2:p.Gly182= | |
NM_002187.2:c.544G= , LRG_71t1:c.544G= | NP_002178.2:p.Gly182= | |
XR_001742945.1:n.10C= | ||
NM_002187.3:c.544G= MANE Select | NP_002178.2:p.Gly182= |