Canonical Allele Identifier: CA1799890151

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86739698C= , CM000670.2:g.86739698C=	GRCh38
NC_000008.10:g.87751926C= , CM000670.1:g.87751926C=	GRCh37
NC_000008.9:g.87821042C=	NCBI36
NG_016980.1:g.8978G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.168G= MANE Select	ENSP00000316605.5:p.Lys56=
ENST00000681746.1:c.168G=	ENSP00000505959.1:p.Lys56=
ENST00000320005.5:c.168G=	ENSP00000316605.5:p.Lys56=
ENST00000519777.1:n.150G=
NM_019098.4:c.168G=	NP_061971.3:p.Lys56=
NM_019098.5:c.168G= MANE Select	NP_061971.3:p.Lys56=