Canonical Allele Identifier: CA1799784130

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575897A= , CM000670.2:g.86575897A=	GRCh38
NC_000008.10:g.87588125A= , CM000670.1:g.87588125A=	GRCh37
NC_000008.9:g.87657241A=	NCBI36
NG_016980.1:g.172779T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.2337T= MANE Select	ENSP00000316605.5:p.Thr779=
ENST00000681546.1:n.2157T=
ENST00000681746.1:c.*748T=	ENSP00000505959.1:n.*748T=
ENST00000320005.5:c.2337T=	ENSP00000316605.5:p.Thr779=
ENST00000517327.5:c.276+2792T=	ENSP00000428329.1:n.276+2792T=
NM_019098.4:c.2337T=	NP_061971.3:p.Thr779=
XM_011517138.1:c.1923T=	XP_011515440.1:p.Thr641=
XM_011517138.2:c.1923T=	XP_011515440.1:p.Thr641=
NM_019098.5:c.2337T= MANE Select	NP_061971.3:p.Thr779=