Canonical Allele Identifier: CA371449855
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668095C>A , CM000670.2:g.86668095C>A GRCh38
NC_000008.10:g.87680323C>A , CM000670.1:g.87680323C>A GRCh37
NC_000008.9:g.87749439C>A NCBI36
NG_016980.1:g.80581G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.567G>T MANE Select ENSP00000316605.5:p.Trp189Cys
ENST00000681746.1:c.567G>T ENSP00000505959.1:p.Trp189Cys
ENST00000320005.5:c.567G>T ENSP00000316605.5:p.Trp189Cys
NM_019098.4:c.567G>T NP_061971.3:p.Trp189Cys
XM_011517138.1:c.153G>T XP_011515440.1:p.Trp51Cys
XM_011517138.2:c.153G>T XP_011515440.1:p.Trp51Cys
NM_019098.5:c.567G>T MANE Select NP_061971.3:p.Trp189Cys