Canonical Allele Identifier: CA8083338

Gene: CNGB1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57920534G>A , CM000678.2:g.57920534G>A	GRCh38
NC_000016.9:g.57954438G>A , CM000678.1:g.57954438G>A	GRCh37
NC_000016.8:g.56511939G>A	NCBI36
NG_016351.1:g.55583C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251102.13:c.1654C>T MANE Select	ENSP00000251102.8:p.Arg552Cys
ENST00000251102.12:c.1654C>T	ENSP00000251102.8:p.Arg552Cys
ENST00000564448.5:c.1636C>T	ENSP00000454633.1:p.Arg546Cys
NM_001286130.1:c.1636C>T	NP_001273059.1:p.Arg546Cys
NM_001297.4:c.1654C>T	NP_001288.3:p.Arg552Cys
XM_006721134.2:c.1654C>T	XP_006721197.1:p.Arg552Cys
XM_011522870.1:c.505C>T	XP_011521172.1:p.Arg169Cys
XR_933629.1:n.86-613G>A
XM_011522870.2:c.505C>T	XP_011521172.1:p.Arg169Cys
NM_001286130.2:c.1636C>T	NP_001273059.1:p.Arg546Cys
NM_001297.5:c.1654C>T MANE Select	NP_001288.3:p.Arg552Cys