Canonical Allele Identifier: CA2781156169

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86667171_86667178del , CM000670.2:g.86667171_86667178del	GRCh38
NC_000008.10:g.87679399_87679406del , CM000670.1:g.87679399_87679406del	GRCh37
NC_000008.9:g.87748515_87748522del	NCBI36
NG_016980.1:g.81498_81505del

Transcript Alleles

HGVS	Amino-acid change
ENST00000320005.6:c.644-45_644-38del MANE Select	ENSP00000316605.5:n.644-45_644-38del
ENST00000681746.1:c.644-45_644-38del	ENSP00000505959.1:n.644-45_644-38del
ENST00000320005.5:c.644-45_644-38del	ENSP00000316605.5:n.644-45_644-38del
NM_019098.4:c.644-45_644-38del	NP_061971.3:n.644-45_644-38del
XM_011517138.1:c.230-45_230-38del	XP_011515440.1:n.230-45_230-38del
XM_011517138.2:c.230-45_230-38del	XP_011515440.1:n.230-45_230-38del
NM_019098.5:c.644-45_644-38del MANE Select	NP_061971.3:n.644-45_644-38del