Canonical Allele Identifier: CA1799889882

Gene: CNGB3

Linked Data

• dbSNP Id: rs1825304450

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86739580dup , CM000670.2:g.86739580dup	GRCh38
NC_000008.10:g.87751808dup , CM000670.1:g.87751808dup	GRCh37
NC_000008.9:g.87820924dup	NCBI36
NG_016980.1:g.9096dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.211+75dup MANE Select	ENSP00000316605.5:n.211+75dup
ENST00000681746.1:c.211+75dup	ENSP00000505959.1:n.211+75dup
ENST00000320005.5:c.211+75dup	ENSP00000316605.5:n.211+75dup
ENST00000519777.1:n.193+75dup
NM_019098.4:c.211+75dup	NP_061971.3:n.211+75dup
NM_019098.5:c.211+75dup MANE Select	NP_061971.3:n.211+75dup