Canonical Allele Identifier: CA347832396

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99012538G>C (hg19) ; chr2:g.98396075G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98396075G>C , CM000664.2:g.98396075G>C	GRCh38
NC_000002.11:g.99012538G>C , CM000664.1:g.99012538G>C	GRCh37
NC_000002.10:g.98378970G>C	NCBI36
NG_009097.1:g.54921G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.905G>C MANE Select	ENSP00000272602.2:p.Arg302Thr
ENST00000272602.6:c.905G>C	ENSP00000272602.2:p.Arg302Thr
ENST00000393504.5:c.905G>C	ENSP00000377140.1:p.Arg302Thr
ENST00000409937.1:c.917G>C	ENSP00000386761.1:p.Arg306Thr
ENST00000436404.6:c.851G>C	ENSP00000410070.2:p.Arg284Thr
NM_001079878.1:c.851G>C	NP_001073347.1:p.Arg284Thr
NM_001298.2:c.905G>C	NP_001289.1:p.Arg302Thr
XM_006712243.2:c.1016G>C	XP_006712306.1:p.Arg339Thr
XM_011510554.1:c.1070G>C	XP_011508856.1:p.Arg357Thr
XM_011510554.2:c.1070G>C	XP_011508856.1:p.Arg357Thr
NM_001079878.2:c.851G>C	NP_001073347.1:p.Arg284Thr
NM_001298.3:c.905G>C MANE Select	NP_001289.1:p.Arg302Thr