Canonical Allele Identifier: CA1969072066

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725958A= , CM000673.2:g.46725958A=	GRCh38
NC_000011.9:g.46747508A= , CM000673.1:g.46747508A=	GRCh37
NC_000011.8:g.46704084A=	NCBI36
NG_008953.1:g.11766A= , LRG_551:g.11766A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.659A= MANE Select	ENSP00000308541.5:p.Gln220=
ENST00000311907.9:c.659A=	ENSP00000308541.5:p.Gln220=
ENST00000442468.1:c.629A=	ENSP00000387413.1:p.Gln210=
ENST00000490274.1:n.439A=
ENST00000530231.5:c.659A=	ENSP00000433907.1:p.Gln220=
NM_000506.3:c.659A=	NP_000497.1:p.Gln220=
NM_000506.4:c.659A= , LRG_551t1:c.659A=	NP_000497.1:p.Gln220=
NM_001311257.1:c.611A=	NP_001298186.1:p.Gln204=
XR_428840.2:n.703A=
XR_428840.4:n.694A=
NM_000506.5:c.659A= MANE Select	NP_000497.1:p.Gln220=
NM_001311257.2:c.611A=	NP_001298186.1:p.Gln204=