Canonical Allele Identifier: CA393814001
Gene: CIB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90231199C>G , CM000677.2:g.90231199C>G GRCh38
NC_000015.9:g.90774431C>G , CM000677.1:g.90774431C>G GRCh37
NC_000015.8:g.88575435C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000695870.1:n.2220G>C
ENST00000695871.1:n.634G>C
ENST00000695872.1:n.393G>C
ENST00000695873.1:n.541G>C
ENST00000695874.1:n.530G>C
ENST00000328649.11:c.361G>C MANE Select ENSP00000333873.6:p.Gly121Arg
ENST00000650306.1:c.-84G>C ENSP00000497451.1:n.-84G>C
ENST00000328649.10:c.361G>C ENSP00000333873.6:p.Gly121Arg
ENST00000612800.1:c.481G>C ENSP00000479860.1:p.Gly161Arg
NM_001277764.1:c.481G>C NP_001264693.1:p.Gly161Arg
NM_006384.3:c.361G>C NP_006375.2:p.Gly121Arg
NR_102427.1:n.547G>C
NR_102428.1:n.413G>C
XM_006720375.1:c.361G>C XP_006720438.1:p.Gly121Arg
XM_006720375.2:c.361G>C XP_006720438.1:p.Gly121Arg
NM_006384.4:c.361G>C MANE Select NP_006375.2:p.Gly121Arg
NM_001277764.2:c.481G>C NP_001264693.1:p.Gly161Arg