Canonical Allele Identifier: CA1799781777

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86574197T= , CM000670.2:g.86574197T=	GRCh38
NC_000008.10:g.87586425T= , CM000670.1:g.87586425T=	GRCh37
NC_000008.9:g.87655541T=	NCBI36
NG_016980.1:g.174479A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.*1607A= MANE Select	ENSP00000316605.5:n.*1607A=
ENST00000681746.1:c.*2448A=	ENSP00000505959.1:n.*2448A=
ENST00000320005.5:c.*1607A=	ENSP00000316605.5:n.*1607A=
ENST00000517327.5:c.276+4492A=	ENSP00000428329.1:n.276+4492A=
NM_019098.4:c.*1607A=	NP_061971.3:n.*1607A=
XM_011517138.1:c.*1607A=	XP_011515440.1:n.*1607A=
XM_011517138.2:c.*1607A=	XP_011515440.1:n.*1607A=
NM_019098.5:c.*1607A= MANE Select	NP_061971.3:n.*1607A=