Canonical Allele Identifier: CA1799830495

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86671499G= , CM000670.2:g.86671499G=	GRCh38
NC_000008.10:g.87683727G= , CM000670.1:g.87683727G=	GRCh37
NC_000008.9:g.87752843G=	NCBI36
NG_016980.1:g.77177C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.339-401C= MANE Select	ENSP00000316605.5:n.339-401C=
ENST00000680314.1:n.100-401C=
ENST00000681746.1:c.339-401C=	ENSP00000505959.1:n.339-401C=
ENST00000320005.5:c.339-401C=	ENSP00000316605.5:n.339-401C=
NM_019098.4:c.339-401C=	NP_061971.3:n.339-401C=
XM_011517138.1:c.-76-401C=	XP_011515440.1:n.-76-401C=
XM_011517138.2:c.-76-401C=	XP_011515440.1:n.-76-401C=
NM_019098.5:c.339-401C= MANE Select	NP_061971.3:n.339-401C=