HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312751G= , CM000673.2:g.118312751G= | GRCh38 |
NC_000011.9:g.118183466G= , CM000673.1:g.118183466G= | GRCh37 |
NC_000011.8:g.117688676G= | NCBI36 |
NG_007383.1:g.13172G= , LRG_38:g.13172G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.237G= MANE Select | ENSP00000354566.4:p.Glu79= | |
ENST00000361763.8:c.237G= | ENSP00000354566.4:p.Glu79= | |
ENST00000526146.5:n.783G= | ||
ENST00000528435.5:n.790G= | ||
ENST00000528600.1:c.219G= | ENSP00000433975.1:p.Glu73= | |
ENST00000529713.5:n.343G= | ||
ENST00000531913.1:n.608G= | ||
NM_000733.3:c.237G= , LRG_38t1:c.237G= | NP_000724.1:p.Glu79= | |
NM_000733.4:c.237G= MANE Select | NP_000724.1:p.Glu79= |