Canonical Allele Identifier: CA1969072681

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726513A= , CM000673.2:g.46726513A=	GRCh38
NC_000011.9:g.46748063A= , CM000673.1:g.46748063A=	GRCh37
NC_000011.8:g.46704639A=	NCBI36
NG_008953.1:g.12321A= , LRG_551:g.12321A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.890A= MANE Select	ENSP00000308541.5:p.Glu297=
ENST00000311907.9:c.890A=	ENSP00000308541.5:p.Glu297=
ENST00000442468.1:c.860A=	ENSP00000387413.1:p.Glu287=
ENST00000530231.5:c.890A=	ENSP00000433907.1:p.Glu297=
NM_000506.3:c.890A=	NP_000497.1:p.Glu297=
NM_000506.4:c.890A= , LRG_551t1:c.890A=	NP_000497.1:p.Glu297=
NM_001311257.1:c.842A=	NP_001298186.1:p.Glu281=
XR_428840.2:n.934A=
XR_428840.4:n.925A=
NM_000506.5:c.890A= MANE Select	NP_000497.1:p.Glu297=
NM_001311257.2:c.842A=	NP_001298186.1:p.Glu281=