Canonical Allele Identifier: CA1799781773

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86574196T= , CM000670.2:g.86574196T=	GRCh38
NC_000008.10:g.87586424T= , CM000670.1:g.87586424T=	GRCh37
NC_000008.9:g.87655540T=	NCBI36
NG_016980.1:g.174480A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320005.6:c.*1608A= MANE Select	ENSP00000316605.5:n.*1608A=
ENST00000681746.1:c.*2449A=	ENSP00000505959.1:n.*2449A=
ENST00000320005.5:c.*1608A=	ENSP00000316605.5:n.*1608A=
ENST00000517327.5:c.276+4493A=	ENSP00000428329.1:n.276+4493A=
NM_019098.4:c.*1608A=	NP_061971.3:n.*1608A=
XM_011517138.1:c.*1608A=	XP_011515440.1:n.*1608A=
XM_011517138.2:c.*1608A=	XP_011515440.1:n.*1608A=
NM_019098.5:c.*1608A= MANE Select	NP_061971.3:n.*1608A=