Canonical Allele Identifier: CA1969071906

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725870G= , CM000673.2:g.46725870G=	GRCh38
NC_000011.9:g.46747420G= , CM000673.1:g.46747420G=	GRCh37
NC_000011.8:g.46703996G=	NCBI36
NG_008953.1:g.11678G= , LRG_551:g.11678G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.571G= MANE Select	ENSP00000308541.5:p.Val191=
ENST00000311907.9:c.571G=	ENSP00000308541.5:p.Val191=
ENST00000442468.1:c.541G=	ENSP00000387413.1:p.Val181=
ENST00000490274.1:n.351G=
ENST00000530231.5:c.571G=	ENSP00000433907.1:p.Val191=
NM_000506.3:c.571G=	NP_000497.1:p.Val191=
NM_000506.4:c.571G= , LRG_551t1:c.571G=	NP_000497.1:p.Val191=
NM_001311257.1:c.523G=	NP_001298186.1:p.Val175=
XR_428840.2:n.615G=
XR_428840.4:n.606G=
NM_000506.5:c.571G= MANE Select	NP_000497.1:p.Val191=
NM_001311257.2:c.523G=	NP_001298186.1:p.Val175=