Canonical Allele Identifier: CA427567049

Gene: CNGA3

Linked Data

• MyVariant Identifiers: chr2:g.99006130G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389667G>T , CM000664.2:g.98389667G>T	GRCh38
NC_000002.11:g.99006130G>T , CM000664.1:g.99006130G>T	GRCh37
NC_000002.10:g.98372562G>T	NCBI36
NG_009097.1:g.48513G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.459G>T MANE Select	ENSP00000272602.2:p.Thr153=
ENST00000272602.6:c.459G>T	ENSP00000272602.2:p.Thr153=
ENST00000393503.2:n.464G>T
ENST00000393504.5:c.459G>T	ENSP00000377140.1:p.Thr153=
ENST00000409937.1:c.471G>T	ENSP00000386761.1:p.Thr157=
ENST00000436404.6:c.405G>T	ENSP00000410070.2:p.Thr135=
NM_001079878.1:c.405G>T	NP_001073347.1:p.Thr135=
NM_001298.2:c.459G>T	NP_001289.1:p.Thr153=
XM_006712243.2:c.570G>T	XP_006712306.1:p.Thr190=
XM_011510554.1:c.624G>T	XP_011508856.1:p.Thr208=
XM_011510554.2:c.624G>T	XP_011508856.1:p.Thr208=
NM_001079878.2:c.405G>T	NP_001073347.1:p.Thr135=
NM_001298.3:c.459G>T MANE Select	NP_001289.1:p.Thr153=