Canonical Allele Identifier: CA7680339
Community Standard Title: NM_006383.4(CIB2):c.87-3A>G
Gene: CIB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78111279T>C , CM000677.2:g.78111279T>C GRCh38
NC_000015.9:g.78403621T>C , CM000677.1:g.78403621T>C GRCh37
NC_000015.8:g.76190676T>C NCBI36
NG_033006.1:g.25257A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006383.4:c.87-3A>G MANE Select NP_006374.1:n.87-3A>G
ENST00000258930.8:c.87-3A>G MANE Select ENSP00000258930.3:n.87-3A>G
NM_001271888.1:c.-43-3A>G NP_001258817.1:n.-43-3A>G
NM_001271888.2:c.-43-3A>G NP_001258817.1:n.-43-3A>G
NM_001271889.1:c.52-1897A>G NP_001258818.1:n.52-1897A>G
NM_001271889.2:c.52-1897A>G NP_001258818.1:n.52-1897A>G
NM_001301224.1:c.87-1770A>G NP_001288153.1:n.87-1770A>G
NM_001301224.2:c.87-1770A>G NP_001288153.1:n.87-1770A>G
NM_006383.3:c.87-3A>G NP_006374.1:n.87-3A>G
NR_125435.1:n.407-1897A>G
NR_125435.2:n.407-1897A>G
ENST00000258930.7:c.87-3A>G ENSP00000258930.3:n.87-3A>G
ENST00000539011.5:c.-43-3A>G ENSP00000442459.1:n.-43-3A>G
ENST00000557846.5:c.52-1897A>G ENSP00000453488.1:n.52-1897A>G
ENST00000557917.5:c.87-1897A>G ENSP00000453963.1:n.87-1897A>G
ENST00000559054.1:c.-43-3A>G ENSP00000453377.1:n.-43-3A>G
ENST00000559645.1:c.87-1770A>G ENSP00000452980.1:n.87-1770A>G
ENST00000560618.5:c.-43-3A>G ENSP00000452752.1:n.-43-3A>G
ENST00000561190.5:c.87-3A>G ENSP00000453256.1:n.87-3A>G
XM_005254126.2:c.87-3A>G XP_005254183.1:n.87-3A>G
XM_005254126.3:c.87-3A>G XP_005254183.1:n.87-3A>G
XM_006720374.2:c.-43-3A>G XP_006720437.1:n.-43-3A>G
XM_011521161.1:c.-43-3A>G XP_011519463.1:n.-43-3A>G
XM_011521161.2:c.-43-3A>G XP_011519463.1:n.-43-3A>G
XR_001751051.1:n.848-3A>G