Canonical Allele Identifier: CA180328059
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs916748731

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86574070G>C , CM000670.2:g.86574070G>C GRCh38
NC_000008.10:g.87586298G>C , CM000670.1:g.87586298G>C GRCh37
NC_000008.9:g.87655414G>C NCBI36
NG_016980.1:g.174606C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000681746.1:c.*2575C>G ENSP00000505959.1:n.*2575C>G
ENST00000320005.5:c.*1734C>G ENSP00000316605.5:n.*1734C>G
ENST00000517327.5:c.276+4619C>G ENSP00000428329.1:n.276+4619C>G
NM_019098.4:c.*1734C>G NP_061971.3:n.*1734C>G
XM_011517138.1:c.*1734C>G XP_011515440.1:n.*1734C>G
XM_011517138.2:c.*1734C>G XP_011515440.1:n.*1734C>G