HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57766051C= , CM000674.2:g.57766051C= | GRCh38 |
NC_000012.11:g.58159834C= , CM000674.1:g.58159834C= | GRCh37 |
NC_000012.10:g.56446101C= | NCBI36 |
NG_007076.1:g.6143G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000546609.2:n.254G= | ||
ENST00000713544.1:c.342G= | ENSP00000518840.1:p.Thr114= | |
ENST00000713545.1:c.342G= | ENSP00000518841.1:p.Thr114= | |
ENST00000228606.9:c.342G= MANE Select | ENSP00000228606.4:p.Thr114= | |
ENST00000228606.8:c.342G= | ENSP00000228606.4:p.Thr114= | |
ENST00000546496.1:n.170G= | ||
ENST00000546609.1:c.254G= | ||
ENST00000547344.5:n.396G= | ||
ENST00000552186.1:n.461G= | ||
NM_000785.3:c.342G= | NP_000776.1:p.Thr114= | |
NM_000785.4:c.342G= MANE Select | NP_000776.1:p.Thr114= |