Canonical Allele Identifier: CA1799890064
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739661T= , CM000670.2:g.86739661T= GRCh38
NC_000008.10:g.87751889T= , CM000670.1:g.87751889T= GRCh37
NC_000008.9:g.87821005T= NCBI36
NG_016980.1:g.9015A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.205A= MANE Select ENSP00000316605.5:p.Ile69=
ENST00000681746.1:c.205A= ENSP00000505959.1:p.Ile69=
ENST00000320005.5:c.205A= ENSP00000316605.5:p.Ile69=
ENST00000519777.1:n.187A=
NM_019098.4:c.205A= NP_061971.3:p.Ile69=
NM_019098.5:c.205A= MANE Select NP_061971.3:p.Ile69=