Canonical Allele Identifier: CA1799783503

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575518T= , CM000670.2:g.86575518T=	GRCh38
NC_000008.10:g.87587746T= , CM000670.1:g.87587746T=	GRCh37
NC_000008.9:g.87656862T=	NCBI36
NG_016980.1:g.173158A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.*286A= MANE Select	ENSP00000316605.5:n.*286A=
ENST00000681546.1:n.2536A=
ENST00000681746.1:c.*1127A=	ENSP00000505959.1:n.*1127A=
ENST00000320005.5:c.*286A=	ENSP00000316605.5:n.*286A=
ENST00000517327.5:c.276+3171A=	ENSP00000428329.1:n.276+3171A=
NM_019098.4:c.*286A=	NP_061971.3:n.*286A=
XM_011517138.1:c.*286A=	XP_011515440.1:n.*286A=
XM_011517138.2:c.*286A=	XP_011515440.1:n.*286A=
NM_019098.5:c.*286A= MANE Select	NP_061971.3:n.*286A=