Canonical Allele Identifier: CA1969072378

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726186G= , CM000673.2:g.46726186G=	GRCh38
NC_000011.9:g.46747736G= , CM000673.1:g.46747736G=	GRCh37
NC_000011.8:g.46704312G=	NCBI36
NG_008953.1:g.11994G= , LRG_551:g.11994G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+13G= MANE Select	ENSP00000308541.5:n.874+13G=
ENST00000311907.9:c.874+13G=	ENSP00000308541.5:n.874+13G=
ENST00000442468.1:c.844+13G=	ENSP00000387413.1:n.844+13G=
ENST00000530231.5:c.874+13G=	ENSP00000433907.1:n.874+13G=
NM_000506.3:c.874+13G=	NP_000497.1:n.874+13G=
NM_000506.4:c.874+13G= , LRG_551t1:c.874+13G=	NP_000497.1:n.874+13G=
NM_001311257.1:c.826+13G=	NP_001298186.1:n.826+13G=
XR_428840.2:n.918+13G=
XR_428840.4:n.909+13G=
NM_000506.5:c.874+13G= MANE Select	NP_000497.1:n.874+13G=
NM_001311257.2:c.826+13G=	NP_001298186.1:n.826+13G=