Canonical Allele Identifier: CA2842323209

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395746G>T , CM000664.2:g.98395746G>T	GRCh38
NC_000002.11:g.99012209G>T , CM000664.1:g.99012209G>T	GRCh37
NC_000002.10:g.98378641G>T	NCBI36
NG_009097.1:g.54592G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.674-98G>T MANE Select	ENSP00000272602.2:n.674-98G>T
ENST00000272602.6:c.674-98G>T	ENSP00000272602.2:n.674-98G>T
ENST00000393504.5:c.674-98G>T	ENSP00000377140.1:n.674-98G>T
ENST00000409937.1:c.686-98G>T	ENSP00000386761.1:n.686-98G>T
ENST00000436404.6:c.620-98G>T	ENSP00000410070.2:n.620-98G>T
NM_001079878.1:c.620-98G>T	NP_001073347.1:n.620-98G>T
NM_001298.2:c.674-98G>T	NP_001289.1:n.674-98G>T
XM_006712243.2:c.785-98G>T	XP_006712306.1:n.785-98G>T
XM_011510554.1:c.839-98G>T	XP_011508856.1:n.839-98G>T
XM_011510554.2:c.839-98G>T	XP_011508856.1:n.839-98G>T
NM_001079878.2:c.620-98G>T	NP_001073347.1:n.620-98G>T
NM_001298.3:c.674-98G>T MANE Select	NP_001289.1:n.674-98G>T