Canonical Allele Identifier: CA347831644

Gene: CNGA3

Linked Data

• dbSNP Id: rs1692740720
• MyVariant Identifiers: chr2:g.99006232T>G (hg19) ; chr2:g.98389769T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389769T>G , CM000664.2:g.98389769T>G	GRCh38
NC_000002.11:g.99006232T>G , CM000664.1:g.99006232T>G	GRCh37
NC_000002.10:g.98372664T>G	NCBI36
NG_009097.1:g.48615T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.561T>G MANE Select	ENSP00000272602.2:p.Ile187Met
ENST00000272602.6:c.561T>G	ENSP00000272602.2:p.Ile187Met
ENST00000393503.2:n.566T>G
ENST00000393504.5:c.561T>G	ENSP00000377140.1:p.Ile187Met
ENST00000409937.1:c.573T>G	ENSP00000386761.1:p.Ile191Met
ENST00000436404.6:c.507T>G	ENSP00000410070.2:p.Ile169Met
NM_001079878.1:c.507T>G	NP_001073347.1:p.Ile169Met
NM_001298.2:c.561T>G	NP_001289.1:p.Ile187Met
XM_006712243.2:c.672T>G	XP_006712306.1:p.Ile224Met
XM_011510554.1:c.726T>G	XP_011508856.1:p.Ile242Met
XM_011510554.2:c.726T>G	XP_011508856.1:p.Ile242Met
NM_001079878.2:c.507T>G	NP_001073347.1:p.Ile169Met
NM_001298.3:c.561T>G MANE Select	NP_001289.1:p.Ile187Met