Canonical Allele Identifier: CA371445992

Gene: CNGB3

Linked Data

• MyVariant Identifiers: chr8:g.87588049C>T (hg19) ; chr8:g.86575821C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575821C>T , CM000670.2:g.86575821C>T	GRCh38
NC_000008.10:g.87588049C>T , CM000670.1:g.87588049C>T	GRCh37
NC_000008.9:g.87657165C>T	NCBI36
NG_016980.1:g.172855G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.2413G>A MANE Select	ENSP00000316605.5:p.Glu805Lys
ENST00000681546.1:n.2233G>A
ENST00000681746.1:c.*824G>A	ENSP00000505959.1:n.*824G>A
ENST00000320005.5:c.2413G>A	ENSP00000316605.5:p.Glu805Lys
ENST00000517327.5:c.276+2868G>A	ENSP00000428329.1:n.276+2868G>A
NM_019098.4:c.2413G>A	NP_061971.3:p.Glu805Lys
XM_011517138.1:c.1999G>A	XP_011515440.1:p.Glu667Lys
XM_011517138.2:c.1999G>A	XP_011515440.1:p.Glu667Lys
NM_019098.5:c.2413G>A MANE Select	NP_061971.3:p.Glu805Lys