Canonical Allele Identifier: CA1969072292

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726147T= , CM000673.2:g.46726147T=	GRCh38
NC_000011.9:g.46747697T= , CM000673.1:g.46747697T=	GRCh37
NC_000011.8:g.46704273T=	NCBI36
NG_008953.1:g.11955T= , LRG_551:g.11955T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.848T= MANE Select	ENSP00000308541.5:p.Phe283=
ENST00000311907.9:c.848T=	ENSP00000308541.5:p.Phe283=
ENST00000442468.1:c.818T=	ENSP00000387413.1:p.Phe273=
ENST00000530231.5:c.848T=	ENSP00000433907.1:p.Phe283=
NM_000506.3:c.848T=	NP_000497.1:p.Phe283=
NM_000506.4:c.848T= , LRG_551t1:c.848T=	NP_000497.1:p.Phe283=
NM_001311257.1:c.800T=	NP_001298186.1:p.Phe267=
XR_428840.2:n.892T=
XR_428840.4:n.883T=
NM_000506.5:c.848T= MANE Select	NP_000497.1:p.Phe283=
NM_001311257.2:c.800T=	NP_001298186.1:p.Phe267=