Canonical Allele Identifier: CA2687823431

Gene: CNGB3

Linked Data

• gnomAD v4: 8-86575522-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575522C>A , CM000670.2:g.86575522C>A	GRCh38
NC_000008.10:g.87587750C>A , CM000670.1:g.87587750C>A	GRCh37
NC_000008.9:g.87656866C>A	NCBI36
NG_016980.1:g.173154G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.*282G>T MANE Select	ENSP00000316605.5:n.*282G>T
ENST00000681546.1:n.2532G>T
ENST00000681746.1:c.*1123G>T	ENSP00000505959.1:n.*1123G>T
ENST00000320005.5:c.*282G>T	ENSP00000316605.5:n.*282G>T
ENST00000517327.5:c.276+3167G>T	ENSP00000428329.1:n.276+3167G>T
NM_019098.4:c.*282G>T	NP_061971.3:n.*282G>T
XM_011517138.1:c.*282G>T	XP_011515440.1:n.*282G>T
XM_011517138.2:c.*282G>T	XP_011515440.1:n.*282G>T
NM_019098.5:c.*282G>T MANE Select	NP_061971.3:n.*282G>T