Canonical Allele Identifier: CA1969071869

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725851C= , CM000673.2:g.46725851C=	GRCh38
NC_000011.9:g.46747401C= , CM000673.1:g.46747401C=	GRCh37
NC_000011.8:g.46703977C=	NCBI36
NG_008953.1:g.11659C= , LRG_551:g.11659C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.560-8C= MANE Select	ENSP00000308541.5:n.560-8C=
ENST00000311907.9:c.560-8C=	ENSP00000308541.5:n.560-8C=
ENST00000442468.1:c.530-8C=	ENSP00000387413.1:n.530-8C=
ENST00000490274.1:n.340-8C=
ENST00000530231.5:c.560-8C=	ENSP00000433907.1:n.560-8C=
NM_000506.3:c.560-8C=	NP_000497.1:n.560-8C=
NM_000506.4:c.560-8C= , LRG_551t1:c.560-8C=	NP_000497.1:n.560-8C=
NM_001311257.1:c.512-8C=	NP_001298186.1:n.512-8C=
XR_428840.2:n.604-8C=
XR_428840.4:n.595-8C=
NM_000506.5:c.560-8C= MANE Select	NP_000497.1:n.560-8C=
NM_001311257.2:c.512-8C=	NP_001298186.1:n.512-8C=