Canonical Allele Identifier: CA1969071943

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725893C= , CM000673.2:g.46725893C=	GRCh38
NC_000011.9:g.46747443C= , CM000673.1:g.46747443C=	GRCh37
NC_000011.8:g.46704019C=	NCBI36
NG_008953.1:g.11701C= , LRG_551:g.11701C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.594C= MANE Select	ENSP00000308541.5:p.Arg198=
ENST00000311907.9:c.594C=	ENSP00000308541.5:p.Arg198=
ENST00000442468.1:c.564C=	ENSP00000387413.1:p.Arg188=
ENST00000490274.1:n.374C=
ENST00000530231.5:c.594C=	ENSP00000433907.1:p.Arg198=
NM_000506.3:c.594C=	NP_000497.1:p.Arg198=
NM_000506.4:c.594C= , LRG_551t1:c.594C=	NP_000497.1:p.Arg198=
NM_001311257.1:c.546C=	NP_001298186.1:p.Arg182=
XR_428840.2:n.638C=
XR_428840.4:n.629C=
NM_000506.5:c.594C= MANE Select	NP_000497.1:p.Arg198=
NM_001311257.2:c.546C=	NP_001298186.1:p.Arg182=