Canonical Allele Identifier: CA371456748
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739708A>T , CM000670.2:g.86739708A>T GRCh38
NC_000008.10:g.87751936A>T , CM000670.1:g.87751936A>T GRCh37
NC_000008.9:g.87821052A>T NCBI36
NG_016980.1:g.8968T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.158T>A MANE Select ENSP00000316605.5:p.Leu53His
ENST00000681746.1:c.158T>A ENSP00000505959.1:p.Leu53His
ENST00000320005.5:c.158T>A ENSP00000316605.5:p.Leu53His
ENST00000519777.1:n.140T>A
NM_019098.4:c.158T>A NP_061971.3:p.Leu53His
NM_019098.5:c.158T>A MANE Select NP_061971.3:p.Leu53His