Canonical Allele Identifier: CA1799825678

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86643769T= , CM000670.2:g.86643769T=	GRCh38
NC_000008.10:g.87655997T= , CM000670.1:g.87655997T=	GRCh37
NC_000008.9:g.87725113T=	NCBI36
NG_016980.1:g.104907A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.1160A= MANE Select	ENSP00000316605.5:p.Tyr387=
ENST00000681546.1:n.980A=
ENST00000681746.1:c.1160A=	ENSP00000505959.1:p.Tyr387=
ENST00000320005.5:c.1160A=	ENSP00000316605.5:p.Tyr387=
NM_019098.4:c.1160A=	NP_061971.3:p.Tyr387=
XM_011517138.1:c.746A=	XP_011515440.1:p.Tyr249=
XM_011517138.2:c.746A=	XP_011515440.1:p.Tyr249=
NM_019098.5:c.1160A= MANE Select	NP_061971.3:p.Tyr387=