Canonical Allele Identifier: CA347831922

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99012318C>G (hg19) ; chr2:g.98395855C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395855C>G , CM000664.2:g.98395855C>G	GRCh38
NC_000002.11:g.99012318C>G , CM000664.1:g.99012318C>G	GRCh37
NC_000002.10:g.98378750C>G	NCBI36
NG_009097.1:g.54701C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.685C>G MANE Select	ENSP00000272602.2:p.Gln229Glu
ENST00000272602.6:c.685C>G	ENSP00000272602.2:p.Gln229Glu
ENST00000393504.5:c.685C>G	ENSP00000377140.1:p.Gln229Glu
ENST00000409937.1:c.697C>G	ENSP00000386761.1:p.Gln233Glu
ENST00000436404.6:c.631C>G	ENSP00000410070.2:p.Gln211Glu
NM_001079878.1:c.631C>G	NP_001073347.1:p.Gln211Glu
NM_001298.2:c.685C>G	NP_001289.1:p.Gln229Glu
XM_006712243.2:c.796C>G	XP_006712306.1:p.Gln266Glu
XM_011510554.1:c.850C>G	XP_011508856.1:p.Gln284Glu
XM_011510554.2:c.850C>G	XP_011508856.1:p.Gln284Glu
NM_001079878.2:c.631C>G	NP_001073347.1:p.Gln211Glu
NM_001298.3:c.685C>G MANE Select	NP_001289.1:p.Gln229Glu