Canonical Allele Identifier: CA1969072528

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726338A= , CM000673.2:g.46726338A=	GRCh38
NC_000011.9:g.46747888A= , CM000673.1:g.46747888A=	GRCh37
NC_000011.8:g.46704464A=	NCBI36
NG_008953.1:g.12146A= , LRG_551:g.12146A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.875-160A= MANE Select	ENSP00000308541.5:n.875-160A=
ENST00000311907.9:c.875-160A=	ENSP00000308541.5:n.875-160A=
ENST00000442468.1:c.845-160A=	ENSP00000387413.1:n.845-160A=
ENST00000530231.5:c.875-160A=	ENSP00000433907.1:n.875-160A=
NM_000506.3:c.875-160A=	NP_000497.1:n.875-160A=
NM_000506.4:c.875-160A= , LRG_551t1:c.875-160A=	NP_000497.1:n.875-160A=
NM_001311257.1:c.827-160A=	NP_001298186.1:n.827-160A=
XR_428840.2:n.919-160A=
XR_428840.4:n.910-160A=
NM_000506.5:c.875-160A= MANE Select	NP_000497.1:n.875-160A=
NM_001311257.2:c.827-160A=	NP_001298186.1:n.827-160A=