Canonical Allele Identifier: CA347831432

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99006129C>G (hg19) ; chr2:g.98389666C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389666C>G , CM000664.2:g.98389666C>G	GRCh38
NC_000002.11:g.99006129C>G , CM000664.1:g.99006129C>G	GRCh37
NC_000002.10:g.98372561C>G	NCBI36
NG_009097.1:g.48512C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.458C>G MANE Select	ENSP00000272602.2:p.Thr153Arg
ENST00000272602.6:c.458C>G	ENSP00000272602.2:p.Thr153Arg
ENST00000393503.2:n.463C>G
ENST00000393504.5:c.458C>G	ENSP00000377140.1:p.Thr153Arg
ENST00000409937.1:c.470C>G	ENSP00000386761.1:p.Thr157Arg
ENST00000436404.6:c.404C>G	ENSP00000410070.2:p.Thr135Arg
NM_001079878.1:c.404C>G	NP_001073347.1:p.Thr135Arg
NM_001298.2:c.458C>G	NP_001289.1:p.Thr153Arg
XM_006712243.2:c.569C>G	XP_006712306.1:p.Thr190Arg
XM_011510554.1:c.623C>G	XP_011508856.1:p.Thr208Arg
XM_011510554.2:c.623C>G	XP_011508856.1:p.Thr208Arg
NM_001079878.2:c.404C>G	NP_001073347.1:p.Thr135Arg
NM_001298.3:c.458C>G MANE Select	NP_001289.1:p.Thr153Arg