Canonical Allele Identifier: CA1799868769

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86632824A= , CM000670.2:g.86632824A=	GRCh38
NC_000008.10:g.87645052A= , CM000670.1:g.87645052A=	GRCh37
NC_000008.9:g.87714168A=	NCBI36
NG_016980.1:g.115852T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320005.6:c.1248T= MANE Select	ENSP00000316605.5:p.Thr416=
ENST00000681546.1:n.1068T=
ENST00000681746.1:c.1248T=	ENSP00000505959.1:p.Thr416=
ENST00000320005.5:c.1248T=	ENSP00000316605.5:p.Thr416=
NM_019098.4:c.1248T=	NP_061971.3:p.Thr416=
XM_011517138.1:c.834T=	XP_011515440.1:p.Thr278=
XM_011517138.2:c.834T=	XP_011515440.1:p.Thr278=
NM_019098.5:c.1248T= MANE Select	NP_061971.3:p.Thr416=