Canonical Allele Identifier: CA1799825849

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86643854A= , CM000670.2:g.86643854A=	GRCh38
NC_000008.10:g.87656082A= , CM000670.1:g.87656082A=	GRCh37
NC_000008.9:g.87725198A=	NCBI36
NG_016980.1:g.104822T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.1075T= MANE Select	ENSP00000316605.5:p.Tyr359=
ENST00000681546.1:n.895T=
ENST00000681746.1:c.1075T=	ENSP00000505959.1:p.Tyr359=
ENST00000320005.5:c.1075T=	ENSP00000316605.5:p.Tyr359=
NM_019098.4:c.1075T=	NP_061971.3:p.Tyr359=
XM_011517138.1:c.661T=	XP_011515440.1:p.Tyr221=
XM_011517138.2:c.661T=	XP_011515440.1:p.Tyr221=
NM_019098.5:c.1075T= MANE Select	NP_061971.3:p.Tyr359=