Canonical Allele Identifier: CA2781156502

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86671177_86671178insA , CM000670.2:g.86671177_86671178insA	GRCh38
NC_000008.10:g.87683405_87683406insA , CM000670.1:g.87683405_87683406insA	GRCh37
NC_000008.9:g.87752521_87752522insA	NCBI36
NG_016980.1:g.77498_77499insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.339-80_339-79insT MANE Select	ENSP00000316605.5:n.339-80_339-79insT
ENST00000680314.1:n.100-80_100-79insT
ENST00000681746.1:c.339-80_339-79insT	ENSP00000505959.1:n.339-80_339-79insT
ENST00000320005.5:c.339-80_339-79insT	ENSP00000316605.5:n.339-80_339-79insT
NM_019098.4:c.339-80_339-79insT	NP_061971.3:n.339-80_339-79insT
XM_011517138.1:c.-76-80_-76-79insT	XP_011515440.1:n.-76-80_-76-79insT
XM_011517138.2:c.-76-80_-76-79insT	XP_011515440.1:n.-76-80_-76-79insT
NM_019098.5:c.339-80_339-79insT MANE Select	NP_061971.3:n.339-80_339-79insT