Canonical Allele Identifier: CA2687826635
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86670948_86670949insC , CM000670.2:g.86670948_86670949insC GRCh38
NC_000008.10:g.87683176_87683177insC , CM000670.1:g.87683176_87683177insC GRCh37
NC_000008.9:g.87752292_87752293insC NCBI36
NG_016980.1:g.77727_77728insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.488_489insG MANE Select ENSP00000316605.5:p.Thr164AsnfsTer15
ENST00000680314.1:n.249_250insG
ENST00000681746.1:c.488_489insG ENSP00000505959.1:p.Thr164AsnfsTer15
ENST00000320005.5:c.488_489insG ENSP00000316605.5:p.Thr164AsnfsTer15
NM_019098.4:c.488_489insG NP_061971.3:p.Thr164AsnfsTer15
XM_011517138.1:c.74_75insG XP_011515440.1:p.Thr26AsnfsTer15
XM_011517138.2:c.74_75insG XP_011515440.1:p.Thr26AsnfsTer15
NM_019098.5:c.488_489insG MANE Select NP_061971.3:p.Thr164AsnfsTer15