Canonical Allele Identifier: CA1969072329

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726168A= , CM000673.2:g.46726168A=	GRCh38
NC_000011.9:g.46747718A= , CM000673.1:g.46747718A=	GRCh37
NC_000011.8:g.46704294A=	NCBI36
NG_008953.1:g.11976A= , LRG_551:g.11976A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.869A= MANE Select	ENSP00000308541.5:p.Tyr290=
ENST00000311907.9:c.869A=	ENSP00000308541.5:p.Tyr290=
ENST00000442468.1:c.839A=	ENSP00000387413.1:p.Tyr280=
ENST00000530231.5:c.869A=	ENSP00000433907.1:p.Tyr290=
NM_000506.3:c.869A=	NP_000497.1:p.Tyr290=
NM_000506.4:c.869A= , LRG_551t1:c.869A=	NP_000497.1:p.Tyr290=
NM_001311257.1:c.821A=	NP_001298186.1:p.Tyr274=
XR_428840.2:n.913A=
XR_428840.4:n.904A=
NM_000506.5:c.869A= MANE Select	NP_000497.1:p.Tyr290=
NM_001311257.2:c.821A=	NP_001298186.1:p.Tyr274=