Canonical Allele Identifier: CA1969072735

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726556C= , CM000673.2:g.46726556C=	GRCh38
NC_000011.9:g.46748106C= , CM000673.1:g.46748106C=	GRCh37
NC_000011.8:g.46704682C=	NCBI36
NG_008953.1:g.12364C= , LRG_551:g.12364C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.933C= MANE Select	ENSP00000308541.5:p.Ile311=
ENST00000311907.9:c.933C=	ENSP00000308541.5:p.Ile311=
ENST00000442468.1:c.903C=	ENSP00000387413.1:p.Ile301=
ENST00000530231.5:c.933C=	ENSP00000433907.1:p.Ile311=
NM_000506.3:c.933C=	NP_000497.1:p.Ile311=
NM_000506.4:c.933C= , LRG_551t1:c.933C=	NP_000497.1:p.Ile311=
NM_001311257.1:c.885C=	NP_001298186.1:p.Ile295=
XR_428840.2:n.977C=
XR_428840.4:n.968C=
NM_000506.5:c.933C= MANE Select	NP_000497.1:p.Ile311=
NM_001311257.2:c.885C=	NP_001298186.1:p.Ile295=