Canonical Allele Identifier: CA1799783608

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575598C= , CM000670.2:g.86575598C=	GRCh38
NC_000008.10:g.87587826C= , CM000670.1:g.87587826C=	GRCh37
NC_000008.9:g.87656942C=	NCBI36
NG_016980.1:g.173078G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.*206G= MANE Select	ENSP00000316605.5:n.*206G=
ENST00000681546.1:n.2456G=
ENST00000681746.1:c.*1047G=	ENSP00000505959.1:n.*1047G=
ENST00000320005.5:c.*206G=	ENSP00000316605.5:n.*206G=
ENST00000517327.5:c.276+3091G=	ENSP00000428329.1:n.276+3091G=
NM_019098.4:c.*206G=	NP_061971.3:n.*206G=
XM_011517138.1:c.*206G=	XP_011515440.1:n.*206G=
XM_011517138.2:c.*206G=	XP_011515440.1:n.*206G=
NM_019098.5:c.*206G= MANE Select	NP_061971.3:n.*206G=