Canonical Allele Identifier: CA2189348246

Gene: CIB2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78111171C= , CM000677.2:g.78111171C=	GRCh38
NC_000015.9:g.78403513C= , CM000677.1:g.78403513C=	GRCh37
NC_000015.8:g.76190568C=	NCBI36
NG_033006.1:g.25365G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006383.4:c.192G= MANE Select	NP_006374.1:p.Glu64=
ENST00000258930.8:c.192G= MANE Select	ENSP00000258930.3:p.Glu64=
NM_001271888.1:c.63G=	NP_001258817.1:p.Glu21=
NM_001271888.2:c.63G=	NP_001258817.1:p.Glu21=
NM_001271889.1:c.52-1789G=	NP_001258818.1:n.52-1789G=
NM_001271889.2:c.52-1789G=	NP_001258818.1:n.52-1789G=
NM_001301224.1:c.87-1662G=	NP_001288153.1:n.87-1662G=
NM_001301224.2:c.87-1662G=	NP_001288153.1:n.87-1662G=
NM_006383.3:c.192G=	NP_006374.1:p.Glu64=
NR_125435.1:n.407-1789G=
NR_125435.2:n.407-1789G=
ENST00000258930.7:c.192G=	ENSP00000258930.3:p.Glu64=
ENST00000539011.5:c.63G=	ENSP00000442459.1:p.Glu21=
ENST00000557818.1:c.96G=	ENSP00000453654.1:p.Glu32=
ENST00000557846.5:c.52-1789G=	ENSP00000453488.1:n.52-1789G=
ENST00000557917.5:c.87-1789G=	ENSP00000453963.1:n.87-1789G=
ENST00000559054.1:c.63G=	ENSP00000453377.1:p.Glu21=
ENST00000559645.1:c.87-1662G=	ENSP00000452980.1:n.87-1662G=
ENST00000560618.5:c.63G=	ENSP00000452752.1:p.Glu21=
ENST00000561190.5:c.192G=	ENSP00000453256.1:p.Glu64=
ENST00000643268.1:c.81G=	ENSP00000494155.1:p.Glu27=
XM_005254126.2:c.192G=	XP_005254183.1:p.Glu64=
XM_005254126.3:c.192G=	XP_005254183.1:p.Glu64=
XM_006720374.2:c.63G=	XP_006720437.1:p.Glu21=
XM_011521161.1:c.63G=	XP_011519463.1:p.Glu21=
XM_011521161.2:c.63G=	XP_011519463.1:p.Glu21=
XR_001751051.1:n.953G=