Canonical Allele Identifier: CA371446025

Gene: CNGB3

Linked Data

• MyVariant Identifiers: chr8:g.87588064T>C (hg19) ; chr8:g.86575836T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575836T>C , CM000670.2:g.86575836T>C	GRCh38
NC_000008.10:g.87588064T>C , CM000670.1:g.87588064T>C	GRCh37
NC_000008.9:g.87657180T>C	NCBI36
NG_016980.1:g.172840A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.2398A>G MANE Select	ENSP00000316605.5:p.Thr800Ala
ENST00000681546.1:n.2218A>G
ENST00000681746.1:c.*809A>G	ENSP00000505959.1:n.*809A>G
ENST00000320005.5:c.2398A>G	ENSP00000316605.5:p.Thr800Ala
ENST00000517327.5:c.276+2853A>G	ENSP00000428329.1:n.276+2853A>G
NM_019098.4:c.2398A>G	NP_061971.3:p.Thr800Ala
XM_011517138.1:c.1984A>G	XP_011515440.1:p.Thr662Ala
XM_011517138.2:c.1984A>G	XP_011515440.1:p.Thr662Ala
NM_019098.5:c.2398A>G MANE Select	NP_061971.3:p.Thr800Ala