Canonical Allele Identifier: CA1799781756

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86574182C= , CM000670.2:g.86574182C=	GRCh38
NC_000008.10:g.87586410C= , CM000670.1:g.87586410C=	GRCh37
NC_000008.9:g.87655526C=	NCBI36
NG_016980.1:g.174494G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.*1622G= MANE Select	ENSP00000316605.5:n.*1622G=
ENST00000681746.1:c.*2463G=	ENSP00000505959.1:n.*2463G=
ENST00000320005.5:c.*1622G=	ENSP00000316605.5:n.*1622G=
ENST00000517327.5:c.276+4507G=	ENSP00000428329.1:n.276+4507G=
NM_019098.4:c.*1622G=	NP_061971.3:n.*1622G=
XM_011517138.1:c.*1622G=	XP_011515440.1:n.*1622G=
XM_011517138.2:c.*1622G=	XP_011515440.1:n.*1622G=
NM_019098.5:c.*1622G= MANE Select	NP_061971.3:n.*1622G=