Canonical Allele Identifier: CA856379577

Gene: CNGB3

Linked Data

• dbSNP Id: rs367633289
• MyVariant Identifiers: chr8:g.87751832T>A (hg19) ; chr8:g.86739604T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86739604T>A , CM000670.2:g.86739604T>A	GRCh38
NC_000008.10:g.87751832T>A , CM000670.1:g.87751832T>A	GRCh37
NC_000008.9:g.87820948T>A	NCBI36
NG_016980.1:g.9072A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.211+51A>T MANE Select	ENSP00000316605.5:n.211+51A>T
ENST00000681746.1:c.211+51A>T	ENSP00000505959.1:n.211+51A>T
ENST00000320005.5:c.211+51A>T	ENSP00000316605.5:n.211+51A>T
ENST00000519777.1:n.193+51A>T
NM_019098.4:c.211+51A>T	NP_061971.3:n.211+51A>T
NM_019098.5:c.211+51A>T MANE Select	NP_061971.3:n.211+51A>T