Canonical Allele Identifier: CA7734321
Gene: CIB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90232318C>T , CM000677.2:g.90232318C>T GRCh38
NC_000015.9:g.90775550C>T , CM000677.1:g.90775550C>T GRCh37
NC_000015.8:g.88576554C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000695870.1:n.1244G>A
ENST00000695872.1:n.128G>A
ENST00000695873.1:n.133G>A
ENST00000695874.1:n.265G>A
ENST00000695875.1:n.117G>A
ENST00000695876.1:n.87G>A
ENST00000328649.11:c.96G>A MANE Select ENSP00000333873.6:p.Arg32=
ENST00000650306.1:c.-454G>A ENSP00000497451.1:n.-454G>A
ENST00000328649.10:c.96G>A ENSP00000333873.6:p.Arg32=
ENST00000612800.1:c.216G>A ENSP00000479860.1:p.Arg72=
NM_001277764.1:c.216G>A NP_001264693.1:p.Arg72=
NM_006384.3:c.96G>A NP_006375.2:p.Arg32=
NR_102427.1:n.282G>A
NR_102428.1:n.148G>A
XM_006720375.1:c.96G>A XP_006720438.1:p.Arg32=
XM_006720375.2:c.96G>A XP_006720438.1:p.Arg32=
NM_006384.4:c.96G>A MANE Select NP_006375.2:p.Arg32=
NM_001277764.2:c.216G>A NP_001264693.1:p.Arg72=