Canonical Allele Identifier: CA1969072046

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725948C= , CM000673.2:g.46725948C=	GRCh38
NC_000011.9:g.46747498C= , CM000673.1:g.46747498C=	GRCh37
NC_000011.8:g.46704074C=	NCBI36
NG_008953.1:g.11756C= , LRG_551:g.11756C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.649C= MANE Select	ENSP00000308541.5:p.Arg217=
ENST00000311907.9:c.649C=	ENSP00000308541.5:p.Arg217=
ENST00000442468.1:c.619C=	ENSP00000387413.1:p.Arg207=
ENST00000490274.1:n.429C=
ENST00000530231.5:c.649C=	ENSP00000433907.1:p.Arg217=
NM_000506.3:c.649C=	NP_000497.1:p.Arg217=
NM_000506.4:c.649C= , LRG_551t1:c.649C=	NP_000497.1:p.Arg217=
NM_001311257.1:c.601C=	NP_001298186.1:p.Arg201=
XR_428840.2:n.693C=
XR_428840.4:n.684C=
NM_000506.5:c.649C= MANE Select	NP_000497.1:p.Arg217=
NM_001311257.2:c.601C=	NP_001298186.1:p.Arg201=