Canonical Allele Identifier: CA1969072443

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726253C= , CM000673.2:g.46726253C=	GRCh38
NC_000011.9:g.46747803C= , CM000673.1:g.46747803C=	GRCh37
NC_000011.8:g.46704379C=	NCBI36
NG_008953.1:g.12061C= , LRG_551:g.12061C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+80C= MANE Select	ENSP00000308541.5:n.874+80C=
ENST00000311907.9:c.874+80C=	ENSP00000308541.5:n.874+80C=
ENST00000442468.1:c.844+80C=	ENSP00000387413.1:n.844+80C=
ENST00000530231.5:c.874+80C=	ENSP00000433907.1:n.874+80C=
NM_000506.3:c.874+80C=	NP_000497.1:n.874+80C=
NM_000506.4:c.874+80C= , LRG_551t1:c.874+80C=	NP_000497.1:n.874+80C=
NM_001311257.1:c.826+80C=	NP_001298186.1:n.826+80C=
XR_428840.2:n.918+80C=
XR_428840.4:n.909+80C=
NM_000506.5:c.874+80C= MANE Select	NP_000497.1:n.874+80C=
NM_001311257.2:c.826+80C=	NP_001298186.1:n.826+80C=