HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57766077C= , CM000674.2:g.57766077C= | GRCh38 |
NC_000012.11:g.58159860C= , CM000674.1:g.58159860C= | GRCh37 |
NC_000012.10:g.56446127C= | NCBI36 |
NG_007076.1:g.6117G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000546609.2:n.228G= | ||
ENST00000713544.1:c.316G= | ENSP00000518840.1:p.Glu106= | |
ENST00000713545.1:c.316G= | ENSP00000518841.1:p.Glu106= | |
ENST00000228606.9:c.316G= MANE Select | ENSP00000228606.4:p.Glu106= | |
ENST00000228606.8:c.316G= | ENSP00000228606.4:p.Glu106= | |
ENST00000546496.1:n.144G= | ||
ENST00000546609.1:c.228G= | ||
ENST00000547344.5:n.370G= | ||
ENST00000552186.1:n.435G= | ||
NM_000785.3:c.316G= | NP_000776.1:p.Glu106= | |
NM_000785.4:c.316G= MANE Select | NP_000776.1:p.Glu106= |