Canonical Allele Identifier: CA1969071952

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725897G= , CM000673.2:g.46725897G=	GRCh38
NC_000011.9:g.46747447G= , CM000673.1:g.46747447G=	GRCh37
NC_000011.8:g.46704023G=	NCBI36
NG_008953.1:g.11705G= , LRG_551:g.11705G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.598G= MANE Select	ENSP00000308541.5:p.Glu200=
ENST00000311907.9:c.598G=	ENSP00000308541.5:p.Glu200=
ENST00000442468.1:c.568G=	ENSP00000387413.1:p.Glu190=
ENST00000490274.1:n.378G=
ENST00000530231.5:c.598G=	ENSP00000433907.1:p.Glu200=
NM_000506.3:c.598G=	NP_000497.1:p.Glu200=
NM_000506.4:c.598G= , LRG_551t1:c.598G=	NP_000497.1:p.Glu200=
NM_001311257.1:c.550G=	NP_001298186.1:p.Glu184=
XR_428840.2:n.642G=
XR_428840.4:n.633G=
NM_000506.5:c.598G= MANE Select	NP_000497.1:p.Glu200=
NM_001311257.2:c.550G=	NP_001298186.1:p.Glu184=