Canonical Allele Identifier: CA1799781855

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86574238A= , CM000670.2:g.86574238A=	GRCh38
NC_000008.10:g.87586466A= , CM000670.1:g.87586466A=	GRCh37
NC_000008.9:g.87655582A=	NCBI36
NG_016980.1:g.174438T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320005.6:c.*1566T= MANE Select	ENSP00000316605.5:n.*1566T=
ENST00000681546.1:n.3816T=
ENST00000681746.1:c.*2407T=	ENSP00000505959.1:n.*2407T=
ENST00000320005.5:c.*1566T=	ENSP00000316605.5:n.*1566T=
ENST00000517327.5:c.276+4451T=	ENSP00000428329.1:n.276+4451T=
NM_019098.4:c.*1566T=	NP_061971.3:n.*1566T=
XM_011517138.1:c.*1566T=	XP_011515440.1:n.*1566T=
XM_011517138.2:c.*1566T=	XP_011515440.1:n.*1566T=
NM_019098.5:c.*1566T= MANE Select	NP_061971.3:n.*1566T=