Canonical Allele Identifier: CA1969072750

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726563C= , CM000673.2:g.46726563C=	GRCh38
NC_000011.9:g.46748113C= , CM000673.1:g.46748113C=	GRCh37
NC_000011.8:g.46704689C=	NCBI36
NG_008953.1:g.12371C= , LRG_551:g.12371C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.940C= MANE Select	ENSP00000308541.5:p.Arg314=
ENST00000311907.9:c.940C=	ENSP00000308541.5:p.Arg314=
ENST00000442468.1:c.910C=	ENSP00000387413.1:p.Arg304=
ENST00000530231.5:c.940C=	ENSP00000433907.1:p.Arg314=
NM_000506.3:c.940C=	NP_000497.1:p.Arg314=
NM_000506.4:c.940C= , LRG_551t1:c.940C=	NP_000497.1:p.Arg314=
NM_001311257.1:c.892C=	NP_001298186.1:p.Arg298=
XR_428840.2:n.984C=
XR_428840.4:n.975C=
NM_000506.5:c.940C= MANE Select	NP_000497.1:p.Arg314=
NM_001311257.2:c.892C=	NP_001298186.1:p.Arg298=