Canonical Allele Identifier: CA1799829892

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86671032C= , CM000670.2:g.86671032C=	GRCh38
NC_000008.10:g.87683260C= , CM000670.1:g.87683260C=	GRCh37
NC_000008.9:g.87752376C=	NCBI36
NG_016980.1:g.77644G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320005.6:c.405G= MANE Select	ENSP00000316605.5:p.Leu135=
ENST00000680314.1:n.166G=
ENST00000681746.1:c.405G=	ENSP00000505959.1:p.Leu135=
ENST00000320005.5:c.405G=	ENSP00000316605.5:p.Leu135=
NM_019098.4:c.405G=	NP_061971.3:p.Leu135=
XM_011517138.1:c.-10G=	XP_011515440.1:n.-10G=
XM_011517138.2:c.-10G=	XP_011515440.1:n.-10G=
NM_019098.5:c.405G= MANE Select	NP_061971.3:p.Leu135=