Canonical Allele Identifier: CA856374118

Gene: CNGB3

Linked Data

• dbSNP Id: rs916748731
• gnomAD v3: 8-86574070-G-A
• gnomAD v4: 8-86574070-G-A
• MyVariant Identifiers: chr8:g.87586298G>A (hg19) ; chr8:g.86574070G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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