Canonical Allele Identifier: CA2781156574

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86671254_86671255insG , CM000670.2:g.86671254_86671255insG	GRCh38
NC_000008.10:g.87683482_87683483insG , CM000670.1:g.87683482_87683483insG	GRCh37
NC_000008.9:g.87752598_87752599insG	NCBI36
NG_016980.1:g.77421_77422insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.339-157_339-156insC MANE Select	ENSP00000316605.5:n.339-157_339-156insC
ENST00000680314.1:n.100-157_100-156insC
ENST00000681746.1:c.339-157_339-156insC	ENSP00000505959.1:n.339-157_339-156insC
ENST00000320005.5:c.339-157_339-156insC	ENSP00000316605.5:n.339-157_339-156insC
NM_019098.4:c.339-157_339-156insC	NP_061971.3:n.339-157_339-156insC
XM_011517138.1:c.-76-157_-76-156insC	XP_011515440.1:n.-76-157_-76-156insC
XM_011517138.2:c.-76-157_-76-156insC	XP_011515440.1:n.-76-157_-76-156insC
NM_019098.5:c.339-157_339-156insC MANE Select	NP_061971.3:n.339-157_339-156insC