Canonical Allele Identifier: CA5966971

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723493G>A , CM000673.2:g.46723493G>A	GRCh38
NC_000011.9:g.46745043G>A , CM000673.1:g.46745043G>A	GRCh37
NC_000011.8:g.46701619G>A	NCBI36
NG_008953.1:g.9301G>A , LRG_551:g.9301G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.534G>A MANE Select	ENSP00000308541.5:p.Arg178=
ENST00000311907.9:c.534G>A	ENSP00000308541.5:p.Arg178=
ENST00000442468.1:c.504G>A	ENSP00000387413.1:p.Arg168=
ENST00000490274.1:n.314G>A
ENST00000530231.5:c.534G>A	ENSP00000433907.1:p.Arg178=
NM_000506.3:c.534G>A	NP_000497.1:p.Arg178=
NM_000506.4:c.534G>A , LRG_551t1:c.534G>A	NP_000497.1:p.Arg178=
NM_001311257.1:c.486G>A	NP_001298186.1:p.Arg162=
XR_428840.2:n.578G>A
XR_428840.4:n.569G>A
NM_000506.5:c.534G>A MANE Select	NP_000497.1:p.Arg178=
NM_001311257.2:c.486G>A	NP_001298186.1:p.Arg162=