Canonical Allele Identifier: CA1969072121

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725992G= , CM000673.2:g.46725992G=	GRCh38
NC_000011.9:g.46747542G= , CM000673.1:g.46747542G=	GRCh37
NC_000011.8:g.46704118G=	NCBI36
NG_008953.1:g.11800G= , LRG_551:g.11800G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.693G= MANE Select	ENSP00000308541.5:p.Gly231=
ENST00000311907.9:c.693G=	ENSP00000308541.5:p.Gly231=
ENST00000442468.1:c.663G=	ENSP00000387413.1:p.Gly221=
ENST00000490274.1:n.473G=
ENST00000530231.5:c.693G=	ENSP00000433907.1:p.Gly231=
NM_000506.3:c.693G=	NP_000497.1:p.Gly231=
NM_000506.4:c.693G= , LRG_551t1:c.693G=	NP_000497.1:p.Gly231=
NM_001311257.1:c.645G=	NP_001298186.1:p.Gly215=
XR_428840.2:n.737G=
XR_428840.4:n.728G=
NM_000506.5:c.693G= MANE Select	NP_000497.1:p.Gly231=
NM_001311257.2:c.645G=	NP_001298186.1:p.Gly215=