Canonical Allele Identifier: CA1273419645

Gene: CNGA3

Linked Data

• dbSNP Id: rs1692897592
• gnomAD v4: 2-98395819-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395819C>A , CM000664.2:g.98395819C>A	GRCh38
NC_000002.11:g.99012282C>A , CM000664.1:g.99012282C>A	GRCh37
NC_000002.10:g.98378714C>A	NCBI36
NG_009097.1:g.54665C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.674-25C>A MANE Select	ENSP00000272602.2:n.674-25C>A
ENST00000272602.6:c.674-25C>A	ENSP00000272602.2:n.674-25C>A
ENST00000393504.5:c.674-25C>A	ENSP00000377140.1:n.674-25C>A
ENST00000409937.1:c.686-25C>A	ENSP00000386761.1:n.686-25C>A
ENST00000436404.6:c.620-25C>A	ENSP00000410070.2:n.620-25C>A
NM_001079878.1:c.620-25C>A	NP_001073347.1:n.620-25C>A
NM_001298.2:c.674-25C>A	NP_001289.1:n.674-25C>A
XM_006712243.2:c.785-25C>A	XP_006712306.1:n.785-25C>A
XM_011510554.1:c.839-25C>A	XP_011508856.1:n.839-25C>A
XM_011510554.2:c.839-25C>A	XP_011508856.1:n.839-25C>A
NM_001079878.2:c.620-25C>A	NP_001073347.1:n.620-25C>A
NM_001298.3:c.674-25C>A MANE Select	NP_001289.1:n.674-25C>A