Canonical Allele Identifier: CA1034132010

Gene: CNGA3

Linked Data

• dbSNP Id: rs1692845392
• gnomAD v3: 2-98393756-A-C
• gnomAD v4: 2-98393756-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98393756A>C , CM000664.2:g.98393756A>C	GRCh38
NC_000002.11:g.99010219A>C , CM000664.1:g.99010219A>C	GRCh37
NC_000002.10:g.98376651A>C	NCBI36
NG_009097.1:g.52602A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.673+1786A>C MANE Select	ENSP00000272602.2:n.673+1786A>C
ENST00000272602.6:c.673+1786A>C	ENSP00000272602.2:n.673+1786A>C
ENST00000393504.5:c.673+1786A>C	ENSP00000377140.1:n.673+1786A>C
ENST00000409937.1:c.685+1786A>C	ENSP00000386761.1:n.685+1786A>C
ENST00000436404.6:c.619+1786A>C	ENSP00000410070.2:n.619+1786A>C
NM_001079878.1:c.619+1786A>C	NP_001073347.1:n.619+1786A>C
NM_001298.2:c.673+1786A>C	NP_001289.1:n.673+1786A>C
XM_006712243.2:c.784+1786A>C	XP_006712306.1:n.784+1786A>C
XM_011510554.1:c.838+1786A>C	XP_011508856.1:n.838+1786A>C
XM_011510554.2:c.838+1786A>C	XP_011508856.1:n.838+1786A>C
NM_001079878.2:c.619+1786A>C	NP_001073347.1:n.619+1786A>C
NM_001298.3:c.673+1786A>C MANE Select	NP_001289.1:n.673+1786A>C