Canonical Allele Identifier: CA1969071730

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725698T= , CM000673.2:g.46725698T=	GRCh38
NC_000011.9:g.46747248T= , CM000673.1:g.46747248T=	GRCh37
NC_000011.8:g.46703824T=	NCBI36
NG_008953.1:g.11506T= , LRG_551:g.11506T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.560-161T= MANE Select	ENSP00000308541.5:n.560-161T=
ENST00000311907.9:c.560-161T=	ENSP00000308541.5:n.560-161T=
ENST00000442468.1:c.530-161T=	ENSP00000387413.1:n.530-161T=
ENST00000490274.1:n.340-161T=
ENST00000530231.5:c.560-161T=	ENSP00000433907.1:n.560-161T=
NM_000506.3:c.560-161T=	NP_000497.1:n.560-161T=
NM_000506.4:c.560-161T= , LRG_551t1:c.560-161T=	NP_000497.1:n.560-161T=
NM_001311257.1:c.512-161T=	NP_001298186.1:n.512-161T=
XR_428840.2:n.604-161T=
XR_428840.4:n.595-161T=
NM_000506.5:c.560-161T= MANE Select	NP_000497.1:n.560-161T=
NM_001311257.2:c.512-161T=	NP_001298186.1:n.512-161T=