Canonical Allele Identifier: CA1969072109

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725979T= , CM000673.2:g.46725979T=	GRCh38
NC_000011.9:g.46747529T= , CM000673.1:g.46747529T=	GRCh37
NC_000011.8:g.46704105T=	NCBI36
NG_008953.1:g.11787T= , LRG_551:g.11787T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.680T= MANE Select	ENSP00000308541.5:p.Val227=
ENST00000311907.9:c.680T=	ENSP00000308541.5:p.Val227=
ENST00000442468.1:c.650T=	ENSP00000387413.1:p.Val217=
ENST00000490274.1:n.460T=
ENST00000530231.5:c.680T=	ENSP00000433907.1:p.Val227=
NM_000506.3:c.680T=	NP_000497.1:p.Val227=
NM_000506.4:c.680T= , LRG_551t1:c.680T=	NP_000497.1:p.Val227=
NM_001311257.1:c.632T=	NP_001298186.1:p.Val211=
XR_428840.2:n.724T=
XR_428840.4:n.715T=
NM_000506.5:c.680T= MANE Select	NP_000497.1:p.Val227=
NM_001311257.2:c.632T=	NP_001298186.1:p.Val211=