Canonical Allele Identifier: CA427820163
Gene: CNGA3 HGNC NCBI

Linked Data

COSMIC: COSM722742
MyVariant Identifiers: chr2:g.99013208C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98396745C>A , CM000664.2:g.98396745C>A GRCh38
NC_000002.11:g.99013208C>A , CM000664.1:g.99013208C>A GRCh37
NC_000002.10:g.98379640C>A NCBI36
NG_009097.1:g.55591C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272602.7:c.1575C>A MANE Select ENSP00000272602.2:p.Gly525=
ENST00000272602.6:c.1575C>A ENSP00000272602.2:p.Gly525=
ENST00000393504.5:c.1575C>A ENSP00000377140.1:p.Gly525=
ENST00000409937.1:c.1587C>A ENSP00000386761.1:p.Gly529=
ENST00000436404.6:c.1521C>A ENSP00000410070.2:p.Gly507=
NM_001079878.1:c.1521C>A NP_001073347.1:p.Gly507=
NM_001298.2:c.1575C>A NP_001289.1:p.Gly525=
XM_006712243.2:c.1686C>A XP_006712306.1:p.Gly562=
XM_011510554.1:c.1740C>A XP_011508856.1:p.Gly580=
XM_011510554.2:c.1740C>A XP_011508856.1:p.Gly580=
NM_001079878.2:c.1521C>A NP_001073347.1:p.Gly507=
NM_001298.3:c.1575C>A MANE Select NP_001289.1:p.Gly525=