Canonical Allele Identifier: CA347834040
Gene: CNGA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98396839G>C , CM000664.2:g.98396839G>C GRCh38
NC_000002.11:g.99013302G>C , CM000664.1:g.99013302G>C GRCh37
NC_000002.10:g.98379734G>C NCBI36
NG_009097.1:g.55685G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000272602.7:c.1669G>C MANE Select ENSP00000272602.2:p.Gly557Arg
ENST00000272602.6:c.1669G>C ENSP00000272602.2:p.Gly557Arg
ENST00000393504.5:c.1669G>C ENSP00000377140.1:p.Gly557Arg
ENST00000409937.1:c.1681G>C ENSP00000386761.1:p.Gly561Arg
ENST00000436404.6:c.1615G>C ENSP00000410070.2:p.Gly539Arg
NM_001079878.1:c.1615G>C NP_001073347.1:p.Gly539Arg
NM_001298.2:c.1669G>C NP_001289.1:p.Gly557Arg
XM_006712243.2:c.1780G>C XP_006712306.1:p.Gly594Arg
XM_011510554.1:c.1834G>C XP_011508856.1:p.Gly612Arg
XM_011510554.2:c.1834G>C XP_011508856.1:p.Gly612Arg
NM_001079878.2:c.1615G>C NP_001073347.1:p.Gly539Arg
NM_001298.3:c.1669G>C MANE Select NP_001289.1:p.Gly557Arg