Canonical Allele Identifier: CA1799829005

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86670580T= , CM000670.2:g.86670580T=	GRCh38
NC_000008.10:g.87682808T= , CM000670.1:g.87682808T=	GRCh37
NC_000008.9:g.87751924T=	NCBI36
NG_016980.1:g.78096A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.493+364A= MANE Select	ENSP00000316605.5:n.493+364A=
ENST00000680314.1:n.254+364A=
ENST00000681746.1:c.493+364A=	ENSP00000505959.1:n.493+364A=
ENST00000320005.5:c.493+364A=	ENSP00000316605.5:n.493+364A=
NM_019098.4:c.493+364A=	NP_061971.3:n.493+364A=
XM_011517138.1:c.79+364A=	XP_011515440.1:n.79+364A=
XM_011517138.2:c.79+364A=	XP_011515440.1:n.79+364A=
NM_019098.5:c.493+364A= MANE Select	NP_061971.3:n.493+364A=