Canonical Allele Identifier: CA1969070258

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723453C= , CM000673.2:g.46723453C=	GRCh38
NC_000011.9:g.46745003C= , CM000673.1:g.46745003C=	GRCh37
NC_000011.8:g.46701579C=	NCBI36
NG_008953.1:g.9261C= , LRG_551:g.9261C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000506.5:c.494C= MANE Select	NP_000497.1:p.Thr165=
ENST00000311907.10:c.494C= MANE Select	ENSP00000308541.5:p.Thr165=
NM_000506.3:c.494C=	NP_000497.1:p.Thr165=
NM_000506.4:c.494C= , LRG_551t1:c.494C=	NP_000497.1:p.Thr165=
NM_001311257.1:c.446C=	NP_001298186.1:p.Thr149=
NM_001311257.2:c.446C=	NP_001298186.1:p.Thr149=
ENST00000311907.9:c.494C=	ENSP00000308541.5:p.Thr165=
ENST00000442468.1:c.464C=	ENSP00000387413.1:p.Thr155=
ENST00000490274.1:n.274C=
ENST00000530231.5:c.494C=	ENSP00000433907.1:p.Thr165=
XR_428840.2:n.538C=
XR_428840.4:n.529C=