Canonical Allele Identifier: CA347834074

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99013318A>C (hg19) ; chr2:g.98396855A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98396855A>C , CM000664.2:g.98396855A>C	GRCh38
NC_000002.11:g.99013318A>C , CM000664.1:g.99013318A>C	GRCh37
NC_000002.10:g.98379750A>C	NCBI36
NG_009097.1:g.55701A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.1685A>C MANE Select	ENSP00000272602.2:p.Asn562Thr
ENST00000272602.6:c.1685A>C	ENSP00000272602.2:p.Asn562Thr
ENST00000393504.5:c.1685A>C	ENSP00000377140.1:p.Asn562Thr
ENST00000409937.1:c.1697A>C	ENSP00000386761.1:p.Asn566Thr
ENST00000436404.6:c.1631A>C	ENSP00000410070.2:p.Asn544Thr
NM_001079878.1:c.1631A>C	NP_001073347.1:p.Asn544Thr
NM_001298.2:c.1685A>C	NP_001289.1:p.Asn562Thr
XM_006712243.2:c.1796A>C	XP_006712306.1:p.Asn599Thr
XM_011510554.1:c.1850A>C	XP_011508856.1:p.Asn617Thr
XM_011510554.2:c.1850A>C	XP_011508856.1:p.Asn617Thr
NM_001079878.2:c.1631A>C	NP_001073347.1:p.Asn544Thr
NM_001298.3:c.1685A>C MANE Select	NP_001289.1:p.Asn562Thr