Canonical Allele Identifier: CA1969071768

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725752G= , CM000673.2:g.46725752G=	GRCh38
NC_000011.9:g.46747302G= , CM000673.1:g.46747302G=	GRCh37
NC_000011.8:g.46703878G=	NCBI36
NG_008953.1:g.11560G= , LRG_551:g.11560G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560-107G= MANE Select	ENSP00000308541.5:n.560-107G=
ENST00000311907.9:c.560-107G=	ENSP00000308541.5:n.560-107G=
ENST00000442468.1:c.530-107G=	ENSP00000387413.1:n.530-107G=
ENST00000490274.1:n.340-107G=
ENST00000530231.5:c.560-107G=	ENSP00000433907.1:n.560-107G=
NM_000506.3:c.560-107G=	NP_000497.1:n.560-107G=
NM_000506.4:c.560-107G= , LRG_551t1:c.560-107G=	NP_000497.1:n.560-107G=
NM_001311257.1:c.512-107G=	NP_001298186.1:n.512-107G=
XR_428840.2:n.604-107G=
XR_428840.4:n.595-107G=
NM_000506.5:c.560-107G= MANE Select	NP_000497.1:n.560-107G=
NM_001311257.2:c.512-107G=	NP_001298186.1:n.512-107G=