Canonical Allele Identifier: CA1969071882

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725859G= , CM000673.2:g.46725859G=	GRCh38
NC_000011.9:g.46747409G= , CM000673.1:g.46747409G=	GRCh37
NC_000011.8:g.46703985G=	NCBI36
NG_008953.1:g.11667G= , LRG_551:g.11667G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560G= MANE Select	ENSP00000308541.5:p.Gly187=
ENST00000311907.9:c.560G=	ENSP00000308541.5:p.Gly187=
ENST00000442468.1:c.530G=	ENSP00000387413.1:p.Gly177=
ENST00000490274.1:n.340G=
ENST00000530231.5:c.560G=	ENSP00000433907.1:p.Gly187=
NM_000506.3:c.560G=	NP_000497.1:p.Gly187=
NM_000506.4:c.560G= , LRG_551t1:c.560G=	NP_000497.1:p.Gly187=
NM_001311257.1:c.512G=	NP_001298186.1:p.Gly171=
XR_428840.2:n.604G=
XR_428840.4:n.595G=
NM_000506.5:c.560G= MANE Select	NP_000497.1:p.Gly187=
NM_001311257.2:c.512G=	NP_001298186.1:p.Gly171=