HGVS | Genome Assembly |
---|---|
NC_000005.10:g.76968591G= , CM000667.2:g.76968591G= | GRCh38 |
NC_000005.9:g.76264416G= , CM000667.1:g.76264416G= | GRCh37 |
NC_000005.8:g.76300172G= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000274368.9:c.812-137G= MANE Select | ENSP00000274368.4:n.812-137G= | |
ENST00000274368.8:c.812-137G= | ENSP00000274368.4:n.812-137G= | |
ENST00000503763.1:n.227-137G= | ||
ENST00000514258.1:n.311+5131G= | ||
NM_001882.3:c.812-137G= | NP_001873.2:n.812-137G= | |
XR_948235.1:n.1111+5131G= | ||
XR_948235.3:n.1091+5131G= | ||
NM_001882.4:c.812-137G= MANE Select | NP_001873.2:n.812-137G= |