Canonical Allele Identifier: CA1799783505

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575521T= , CM000670.2:g.86575521T=	GRCh38
NC_000008.10:g.87587749T= , CM000670.1:g.87587749T=	GRCh37
NC_000008.9:g.87656865T=	NCBI36
NG_016980.1:g.173155A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.*283A= MANE Select	ENSP00000316605.5:n.*283A=
ENST00000681546.1:n.2533A=
ENST00000681746.1:c.*1124A=	ENSP00000505959.1:n.*1124A=
ENST00000320005.5:c.*283A=	ENSP00000316605.5:n.*283A=
ENST00000517327.5:c.276+3168A=	ENSP00000428329.1:n.276+3168A=
NM_019098.4:c.*283A=	NP_061971.3:n.*283A=
XM_011517138.1:c.*283A=	XP_011515440.1:n.*283A=
XM_011517138.2:c.*283A=	XP_011515440.1:n.*283A=
NM_019098.5:c.*283A= MANE Select	NP_061971.3:n.*283A=