Canonical Allele Identifier: CA1969072685

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726515G= , CM000673.2:g.46726515G=	GRCh38
NC_000011.9:g.46748065G= , CM000673.1:g.46748065G=	GRCh37
NC_000011.8:g.46704641G=	NCBI36
NG_008953.1:g.12323G= , LRG_551:g.12323G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.892G= MANE Select	ENSP00000308541.5:p.Glu298=
ENST00000311907.9:c.892G=	ENSP00000308541.5:p.Glu298=
ENST00000442468.1:c.862G=	ENSP00000387413.1:p.Glu288=
ENST00000530231.5:c.892G=	ENSP00000433907.1:p.Glu298=
NM_000506.3:c.892G=	NP_000497.1:p.Glu298=
NM_000506.4:c.892G= , LRG_551t1:c.892G=	NP_000497.1:p.Glu298=
NM_001311257.1:c.844G=	NP_001298186.1:p.Glu282=
XR_428840.2:n.936G=
XR_428840.4:n.927G=
NM_000506.5:c.892G= MANE Select	NP_000497.1:p.Glu298=
NM_001311257.2:c.844G=	NP_001298186.1:p.Glu282=