Canonical Allele Identifier: CA347831624

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99006222A>T (hg19) ; chr2:g.98389759A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389759A>T , CM000664.2:g.98389759A>T	GRCh38
NC_000002.11:g.99006222A>T , CM000664.1:g.99006222A>T	GRCh37
NC_000002.10:g.98372654A>T	NCBI36
NG_009097.1:g.48605A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.551A>T MANE Select	ENSP00000272602.2:p.Tyr184Phe
ENST00000272602.6:c.551A>T	ENSP00000272602.2:p.Tyr184Phe
ENST00000393503.2:n.556A>T
ENST00000393504.5:c.551A>T	ENSP00000377140.1:p.Tyr184Phe
ENST00000409937.1:c.563A>T	ENSP00000386761.1:p.Tyr188Phe
ENST00000436404.6:c.497A>T	ENSP00000410070.2:p.Tyr166Phe
NM_001079878.1:c.497A>T	NP_001073347.1:p.Tyr166Phe
NM_001298.2:c.551A>T	NP_001289.1:p.Tyr184Phe
XM_006712243.2:c.662A>T	XP_006712306.1:p.Tyr221Phe
XM_011510554.1:c.716A>T	XP_011508856.1:p.Tyr239Phe
XM_011510554.2:c.716A>T	XP_011508856.1:p.Tyr239Phe
NM_001079878.2:c.497A>T	NP_001073347.1:p.Tyr166Phe
NM_001298.3:c.551A>T MANE Select	NP_001289.1:p.Tyr184Phe