Canonical Allele Identifier: CA1969072720

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726548A= , CM000673.2:g.46726548A=	GRCh38
NC_000011.9:g.46748098A= , CM000673.1:g.46748098A=	GRCh37
NC_000011.8:g.46704674A=	NCBI36
NG_008953.1:g.12356A= , LRG_551:g.12356A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.925A= MANE Select	ENSP00000308541.5:p.Arg309=
ENST00000311907.9:c.925A=	ENSP00000308541.5:p.Arg309=
ENST00000442468.1:c.895A=	ENSP00000387413.1:p.Arg299=
ENST00000530231.5:c.925A=	ENSP00000433907.1:p.Arg309=
NM_000506.3:c.925A=	NP_000497.1:p.Arg309=
NM_000506.4:c.925A= , LRG_551t1:c.925A=	NP_000497.1:p.Arg309=
NM_001311257.1:c.877A=	NP_001298186.1:p.Arg293=
XR_428840.2:n.969A=
XR_428840.4:n.960A=
NM_000506.5:c.925A= MANE Select	NP_000497.1:p.Arg309=
NM_001311257.2:c.877A=	NP_001298186.1:p.Arg293=