Canonical Allele Identifier: CA371456776
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739720T>A , CM000670.2:g.86739720T>A GRCh38
NC_000008.10:g.87751948T>A , CM000670.1:g.87751948T>A GRCh37
NC_000008.9:g.87821064T>A NCBI36
NG_016980.1:g.8956A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.146A>T MANE Select ENSP00000316605.5:p.Glu49Val
ENST00000681746.1:c.146A>T ENSP00000505959.1:p.Glu49Val
ENST00000320005.5:c.146A>T ENSP00000316605.5:p.Glu49Val
ENST00000519777.1:n.128A>T
NM_019098.4:c.146A>T NP_061971.3:p.Glu49Val
NM_019098.5:c.146A>T MANE Select NP_061971.3:p.Glu49Val