Canonical Allele Identifier: CA371456754
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1348237273
gnomAD v2: 8-87751939-G-T
gnomAD v4: 8-86739711-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739711G>T , CM000670.2:g.86739711G>T GRCh38
NC_000008.10:g.87751939G>T , CM000670.1:g.87751939G>T GRCh37
NC_000008.9:g.87821055G>T NCBI36
NG_016980.1:g.8965C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.155C>A MANE Select ENSP00000316605.5:p.Ser52Tyr
ENST00000681746.1:c.155C>A ENSP00000505959.1:p.Ser52Tyr
ENST00000320005.5:c.155C>A ENSP00000316605.5:p.Ser52Tyr
ENST00000519777.1:n.137C>A
NM_019098.4:c.155C>A NP_061971.3:p.Ser52Tyr
NM_019098.5:c.155C>A MANE Select NP_061971.3:p.Ser52Tyr