Canonical Allele Identifier: CA1799782183

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86574484A= , CM000670.2:g.86574484A=	GRCh38
NC_000008.10:g.87586712A= , CM000670.1:g.87586712A=	GRCh37
NC_000008.9:g.87655828A=	NCBI36
NG_016980.1:g.174192T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320005.6:c.*1320T= MANE Select	ENSP00000316605.5:n.*1320T=
ENST00000681546.1:n.3570T=
ENST00000681746.1:c.*2161T=	ENSP00000505959.1:n.*2161T=
ENST00000320005.5:c.*1320T=	ENSP00000316605.5:n.*1320T=
ENST00000517327.5:c.276+4205T=	ENSP00000428329.1:n.276+4205T=
NM_019098.4:c.*1320T=	NP_061971.3:n.*1320T=
XM_011517138.1:c.*1320T=	XP_011515440.1:n.*1320T=
XM_011517138.2:c.*1320T=	XP_011515440.1:n.*1320T=
NM_019098.5:c.*1320T= MANE Select	NP_061971.3:n.*1320T=