Canonical Allele Identifier: CA371446581

Gene: CNGB3

Linked Data

• MyVariant Identifiers: chr8:g.87588316T>A (hg19) ; chr8:g.86576088T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86576088T>A , CM000670.2:g.86576088T>A	GRCh38
NC_000008.10:g.87588316T>A , CM000670.1:g.87588316T>A	GRCh37
NC_000008.9:g.87657432T>A	NCBI36
NG_016980.1:g.172588A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.2146A>T MANE Select	ENSP00000316605.5:p.Asn716Tyr
ENST00000681546.1:n.1966A>T
ENST00000681746.1:c.*557A>T	ENSP00000505959.1:n.*557A>T
ENST00000320005.5:c.2146A>T	ENSP00000316605.5:p.Asn716Tyr
ENST00000517327.5:c.276+2601A>T	ENSP00000428329.1:n.276+2601A>T
NM_019098.4:c.2146A>T	NP_061971.3:p.Asn716Tyr
XM_011517138.1:c.1732A>T	XP_011515440.1:p.Asn578Tyr
XM_011517138.2:c.1732A>T	XP_011515440.1:p.Asn578Tyr
NM_019098.5:c.2146A>T MANE Select	NP_061971.3:p.Asn716Tyr