Canonical Allele Identifier: CA461978634
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86739716-C-T
MyVariant Identifiers: chr8:g.87751944C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739716C>T , CM000670.2:g.86739716C>T GRCh38
NC_000008.10:g.87751944C>T , CM000670.1:g.87751944C>T GRCh37
NC_000008.9:g.87821060C>T NCBI36
NG_016980.1:g.8960G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.150G>A MANE Select ENSP00000316605.5:p.Glu50=
ENST00000681746.1:c.150G>A ENSP00000505959.1:p.Glu50=
ENST00000320005.5:c.150G>A ENSP00000316605.5:p.Glu50=
ENST00000519777.1:n.132G>A
NM_019098.4:c.150G>A NP_061971.3:p.Glu50=
NM_019098.5:c.150G>A MANE Select NP_061971.3:p.Glu50=