Canonical Allele Identifier: CA2781156263

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86668215T>A , CM000670.2:g.86668215T>A	GRCh38
NC_000008.10:g.87680443T>A , CM000670.1:g.87680443T>A	GRCh37
NC_000008.9:g.87749559T>A	NCBI36
NG_016980.1:g.80461A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.494-47A>T MANE Select	ENSP00000316605.5:n.494-47A>T
ENST00000680314.1:n.255-47A>T
ENST00000681746.1:c.494-47A>T	ENSP00000505959.1:n.494-47A>T
ENST00000320005.5:c.494-47A>T	ENSP00000316605.5:n.494-47A>T
NM_019098.4:c.494-47A>T	NP_061971.3:n.494-47A>T
XM_011517138.1:c.80-47A>T	XP_011515440.1:n.80-47A>T
XM_011517138.2:c.80-47A>T	XP_011515440.1:n.80-47A>T
NM_019098.5:c.494-47A>T MANE Select	NP_061971.3:n.494-47A>T