Canonical Allele Identifier: CA393547606
Gene: CIB2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000258930.8:c.192G>T MANE Select ENSP00000258930.3:p.Glu64Asp
ENST00000643268.1:c.81G>T ENSP00000494155.1:p.Glu27Asp
ENST00000258930.7:c.192G>T ENSP00000258930.3:p.Glu64Asp
ENST00000539011.5:c.63G>T ENSP00000442459.1:p.Glu21Asp
ENST00000557818.1:c.96G>T ENSP00000453654.1:p.Glu32Asp
ENST00000557846.5:c.52-1789G>T ENSP00000453488.1:n.52-1789G>T
ENST00000557917.5:c.87-1789G>T ENSP00000453963.1:n.87-1789G>T
ENST00000559054.1:c.63G>T ENSP00000453377.1:p.Glu21Asp
ENST00000559645.1:c.87-1662G>T ENSP00000452980.1:n.87-1662G>T
ENST00000560618.5:c.63G>T ENSP00000452752.1:p.Glu21Asp
ENST00000561190.5:c.192G>T ENSP00000453256.1:p.Glu64Asp
NM_001271888.1:c.63G>T NP_001258817.1:p.Glu21Asp
NM_001271889.1:c.52-1789G>T NP_001258818.1:n.52-1789G>T
NM_001301224.1:c.87-1662G>T NP_001288153.1:n.87-1662G>T
NM_006383.3:c.192G>T NP_006374.1:p.Glu64Asp
NR_125435.1:n.407-1789G>T
XM_005254126.2:c.192G>T XP_005254183.1:p.Glu64Asp
XM_006720374.2:c.63G>T XP_006720437.1:p.Glu21Asp
XM_011521161.1:c.63G>T XP_011519463.1:p.Glu21Asp
XM_005254126.3:c.192G>T XP_005254183.1:p.Glu64Asp
XM_011521161.2:c.63G>T XP_011519463.1:p.Glu21Asp
XR_001751051.1:n.953G>T
NM_001271888.2:c.63G>T NP_001258817.1:p.Glu21Asp
NM_001271889.2:c.52-1789G>T NP_001258818.1:n.52-1789G>T
NM_001301224.2:c.87-1662G>T NP_001288153.1:n.87-1662G>T
NM_006383.4:c.192G>T MANE Select NP_006374.1:p.Glu64Asp
NR_125435.2:n.407-1789G>T