Canonical Allele Identifier: CA427567111

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99006229T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389766T>G , CM000664.2:g.98389766T>G	GRCh38
NC_000002.11:g.99006229T>G , CM000664.1:g.99006229T>G	GRCh37
NC_000002.10:g.98372661T>G	NCBI36
NG_009097.1:g.48612T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.558T>G MANE Select	ENSP00000272602.2:p.Leu186=
ENST00000272602.6:c.558T>G	ENSP00000272602.2:p.Leu186=
ENST00000393503.2:n.563T>G
ENST00000393504.5:c.558T>G	ENSP00000377140.1:p.Leu186=
ENST00000409937.1:c.570T>G	ENSP00000386761.1:p.Leu190=
ENST00000436404.6:c.504T>G	ENSP00000410070.2:p.Leu168=
NM_001079878.1:c.504T>G	NP_001073347.1:p.Leu168=
NM_001298.2:c.558T>G	NP_001289.1:p.Leu186=
XM_006712243.2:c.669T>G	XP_006712306.1:p.Leu223=
XM_011510554.1:c.723T>G	XP_011508856.1:p.Leu241=
XM_011510554.2:c.723T>G	XP_011508856.1:p.Leu241=
NM_001079878.2:c.504T>G	NP_001073347.1:p.Leu168=
NM_001298.3:c.558T>G MANE Select	NP_001289.1:p.Leu186=