Canonical Allele Identifier: CA347831941

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99012327A>G (hg19) ; chr2:g.98395864A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395864A>G , CM000664.2:g.98395864A>G	GRCh38
NC_000002.11:g.99012327A>G , CM000664.1:g.99012327A>G	GRCh37
NC_000002.10:g.98378759A>G	NCBI36
NG_009097.1:g.54710A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.694A>G MANE Select	ENSP00000272602.2:p.Met232Val
ENST00000272602.6:c.694A>G	ENSP00000272602.2:p.Met232Val
ENST00000393504.5:c.694A>G	ENSP00000377140.1:p.Met232Val
ENST00000409937.1:c.706A>G	ENSP00000386761.1:p.Met236Val
ENST00000436404.6:c.640A>G	ENSP00000410070.2:p.Met214Val
NM_001079878.1:c.640A>G	NP_001073347.1:p.Met214Val
NM_001298.2:c.694A>G	NP_001289.1:p.Met232Val
XM_006712243.2:c.805A>G	XP_006712306.1:p.Met269Val
XM_011510554.1:c.859A>G	XP_011508856.1:p.Met287Val
XM_011510554.2:c.859A>G	XP_011508856.1:p.Met287Val
NM_001079878.2:c.640A>G	NP_001073347.1:p.Met214Val
NM_001298.3:c.694A>G MANE Select	NP_001289.1:p.Met232Val