Canonical Allele Identifier: CA427568009

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99012323C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395860C>G , CM000664.2:g.98395860C>G	GRCh38
NC_000002.11:g.99012323C>G , CM000664.1:g.99012323C>G	GRCh37
NC_000002.10:g.98378755C>G	NCBI36
NG_009097.1:g.54706C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.690C>G MANE Select	ENSP00000272602.2:p.Gly230=
ENST00000272602.6:c.690C>G	ENSP00000272602.2:p.Gly230=
ENST00000393504.5:c.690C>G	ENSP00000377140.1:p.Gly230=
ENST00000409937.1:c.702C>G	ENSP00000386761.1:p.Gly234=
ENST00000436404.6:c.636C>G	ENSP00000410070.2:p.Gly212=
NM_001079878.1:c.636C>G	NP_001073347.1:p.Gly212=
NM_001298.2:c.690C>G	NP_001289.1:p.Gly230=
XM_006712243.2:c.801C>G	XP_006712306.1:p.Gly267=
XM_011510554.1:c.855C>G	XP_011508856.1:p.Gly285=
XM_011510554.2:c.855C>G	XP_011508856.1:p.Gly285=
NM_001079878.2:c.636C>G	NP_001073347.1:p.Gly212=
NM_001298.3:c.690C>G MANE Select	NP_001289.1:p.Gly230=