Canonical Allele Identifier: CA2189373592

Gene: CIB2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78105913A= , CM000677.2:g.78105913A=	GRCh38
NC_000015.9:g.78398255A= , CM000677.1:g.78398255A=	GRCh37
NC_000015.8:g.76185310A=	NCBI36
NG_033006.1:g.30623T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258930.8:c.368T= MANE Select	ENSP00000258930.3:p.Ile123=
ENST00000643268.1:c.384T=	ENSP00000494155.1:n.384T=
ENST00000258930.7:c.368T=	ENSP00000258930.3:p.Ile123=
ENST00000539011.5:c.239T=	ENSP00000442459.1:p.Ile80=
ENST00000557818.1:c.350T=	ENSP00000453654.1:n.350T=
ENST00000557846.5:c.221T=	ENSP00000453488.1:p.Ile74=
ENST00000557917.5:c.256T=	ENSP00000453963.1:p.Ser86=
ENST00000559645.1:c.383T=	ENSP00000452980.1:p.Ile128=
ENST00000560618.5:c.239T=	ENSP00000452752.1:p.Ile80=
ENST00000561190.5:c.347-581T=	ENSP00000453256.1:n.347-581T=
NM_001271888.1:c.239T=	NP_001258817.1:p.Ile80=
NM_001271889.1:c.221T=	NP_001258818.1:p.Ile74=
NM_001301224.1:c.383T=	NP_001288153.1:p.Ile128=
NM_006383.3:c.368T=	NP_006374.1:p.Ile123=
NR_125435.1:n.576T=
XM_005254126.2:c.368T=	XP_005254183.1:p.Ile123=
XM_006720374.2:c.239T=	XP_006720437.1:p.Ile80=
XM_011521161.1:c.239T=	XP_011519463.1:p.Ile80=
XM_005254126.3:c.368T=	XP_005254183.1:p.Ile123=
XM_011521161.2:c.239T=	XP_011519463.1:p.Ile80=
XR_001751051.1:n.1256T=
NM_001271888.2:c.239T=	NP_001258817.1:p.Ile80=
NM_001271889.2:c.221T=	NP_001258818.1:p.Ile74=
NM_001301224.2:c.383T=	NP_001288153.1:p.Ile128=
NM_006383.4:c.368T= MANE Select	NP_006374.1:p.Ile123=
NR_125435.2:n.576T=