Canonical Allele Identifier: CA1969072689

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726519C= , CM000673.2:g.46726519C=	GRCh38
NC_000011.9:g.46748069C= , CM000673.1:g.46748069C=	GRCh37
NC_000011.8:g.46704645C=	NCBI36
NG_008953.1:g.12327C= , LRG_551:g.12327C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.896C= MANE Select	ENSP00000308541.5:p.Thr299=
ENST00000311907.9:c.896C=	ENSP00000308541.5:p.Thr299=
ENST00000442468.1:c.866C=	ENSP00000387413.1:p.Thr289=
ENST00000530231.5:c.896C=	ENSP00000433907.1:p.Thr299=
NM_000506.3:c.896C=	NP_000497.1:p.Thr299=
NM_000506.4:c.896C= , LRG_551t1:c.896C=	NP_000497.1:p.Thr299=
NM_001311257.1:c.848C=	NP_001298186.1:p.Thr283=
XR_428840.2:n.940C=
XR_428840.4:n.931C=
NM_000506.5:c.896C= MANE Select	NP_000497.1:p.Thr299=
NM_001311257.2:c.848C=	NP_001298186.1:p.Thr283=