Canonical Allele Identifier: CA347834071

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99013317A>C (hg19) ; chr2:g.98396854A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98396854A>C , CM000664.2:g.98396854A>C	GRCh38
NC_000002.11:g.99013317A>C , CM000664.1:g.99013317A>C	GRCh37
NC_000002.10:g.98379749A>C	NCBI36
NG_009097.1:g.55700A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.1684A>C MANE Select	ENSP00000272602.2:p.Asn562His
ENST00000272602.6:c.1684A>C	ENSP00000272602.2:p.Asn562His
ENST00000393504.5:c.1684A>C	ENSP00000377140.1:p.Asn562His
ENST00000409937.1:c.1696A>C	ENSP00000386761.1:p.Asn566His
ENST00000436404.6:c.1630A>C	ENSP00000410070.2:p.Asn544His
NM_001079878.1:c.1630A>C	NP_001073347.1:p.Asn544His
NM_001298.2:c.1684A>C	NP_001289.1:p.Asn562His
XM_006712243.2:c.1795A>C	XP_006712306.1:p.Asn599His
XM_011510554.1:c.1849A>C	XP_011508856.1:p.Asn617His
XM_011510554.2:c.1849A>C	XP_011508856.1:p.Asn617His
NM_001079878.2:c.1630A>C	NP_001073347.1:p.Asn544His
NM_001298.3:c.1684A>C MANE Select	NP_001289.1:p.Asn562His