Canonical Allele Identifier: CA2781156472

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86671152_86671153insAC , CM000670.2:g.86671152_86671153insAC	GRCh38
NC_000008.10:g.87683380_87683381insAC , CM000670.1:g.87683380_87683381insAC	GRCh37
NC_000008.9:g.87752496_87752497insAC	NCBI36
NG_016980.1:g.77523_77524insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.339-55_339-54insGT MANE Select	ENSP00000316605.5:n.339-55_339-54insGT
ENST00000680314.1:n.100-55_100-54insGT
ENST00000681746.1:c.339-55_339-54insGT	ENSP00000505959.1:n.339-55_339-54insGT
ENST00000320005.5:c.339-55_339-54insGT	ENSP00000316605.5:n.339-55_339-54insGT
NM_019098.4:c.339-55_339-54insGT	NP_061971.3:n.339-55_339-54insGT
XM_011517138.1:c.-76-55_-76-54insGT	XP_011515440.1:n.-76-55_-76-54insGT
XM_011517138.2:c.-76-55_-76-54insGT	XP_011515440.1:n.-76-55_-76-54insGT
NM_019098.5:c.339-55_339-54insGT MANE Select	NP_061971.3:n.339-55_339-54insGT