Canonical Allele Identifier: CA1799829694

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86670977C= , CM000670.2:g.86670977C=	GRCh38
NC_000008.10:g.87683205C= , CM000670.1:g.87683205C=	GRCh37
NC_000008.9:g.87752321C=	NCBI36
NG_016980.1:g.77699G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.460G= MANE Select	ENSP00000316605.5:p.Asp154=
ENST00000680314.1:n.221G=
ENST00000681746.1:c.460G=	ENSP00000505959.1:p.Asp154=
ENST00000320005.5:c.460G=	ENSP00000316605.5:p.Asp154=
NM_019098.4:c.460G=	NP_061971.3:p.Asp154=
XM_011517138.1:c.46G=	XP_011515440.1:p.Asp16=
XM_011517138.2:c.46G=	XP_011515440.1:p.Asp16=
NM_019098.5:c.460G= MANE Select	NP_061971.3:p.Asp154=