Canonical Allele Identifier: CA5966889

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46720809G>A , CM000673.2:g.46720809G>A	GRCh38
NC_000011.9:g.46742359G>A , CM000673.1:g.46742359G>A	GRCh37
NC_000011.8:g.46698935G>A	NCBI36
NG_008953.1:g.6617G>A , LRG_551:g.6617G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000506.5:c.285G>A MANE Select	NP_000497.1:p.Thr95=
ENST00000311907.10:c.285G>A MANE Select	ENSP00000308541.5:p.Thr95=
NM_000506.3:c.285G>A	NP_000497.1:p.Thr95=
NM_000506.4:c.285G>A , LRG_551t1:c.285G>A	NP_000497.1:p.Thr95=
NM_001311257.1:c.237G>A	NP_001298186.1:p.Thr79=
NM_001311257.2:c.237G>A	NP_001298186.1:p.Thr79=
ENST00000311907.9:c.285G>A	ENSP00000308541.5:p.Thr95=
ENST00000442468.1:c.255G>A	ENSP00000387413.1:p.Thr85=
ENST00000530231.5:c.285G>A	ENSP00000433907.1:p.Thr95=
XR_428840.2:n.329G>A
XR_428840.4:n.320G>A