Canonical Allele Identifier: CA1969071930

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725886C= , CM000673.2:g.46725886C=	GRCh38
NC_000011.9:g.46747436C= , CM000673.1:g.46747436C=	GRCh37
NC_000011.8:g.46704012C=	NCBI36
NG_008953.1:g.11694C= , LRG_551:g.11694C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.587C= MANE Select	ENSP00000308541.5:p.Thr196=
ENST00000311907.9:c.587C=	ENSP00000308541.5:p.Thr196=
ENST00000442468.1:c.557C=	ENSP00000387413.1:p.Thr186=
ENST00000490274.1:n.367C=
ENST00000530231.5:c.587C=	ENSP00000433907.1:p.Thr196=
NM_000506.3:c.587C=	NP_000497.1:p.Thr196=
NM_000506.4:c.587C= , LRG_551t1:c.587C=	NP_000497.1:p.Thr196=
NM_001311257.1:c.539C=	NP_001298186.1:p.Thr180=
XR_428840.2:n.631C=
XR_428840.4:n.622C=
NM_000506.5:c.587C= MANE Select	NP_000497.1:p.Thr196=
NM_001311257.2:c.539C=	NP_001298186.1:p.Thr180=