Canonical Allele Identifier: CA462114165

Gene: CNGB3

Linked Data

• MyVariant Identifiers: chr8:g.87588161G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575933G>T , CM000670.2:g.86575933G>T	GRCh38
NC_000008.10:g.87588161G>T , CM000670.1:g.87588161G>T	GRCh37
NC_000008.9:g.87657277G>T	NCBI36
NG_016980.1:g.172743C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.2301C>A MANE Select	ENSP00000316605.5:p.Pro767=
ENST00000681546.1:n.2121C>A
ENST00000681746.1:c.*712C>A	ENSP00000505959.1:n.*712C>A
ENST00000320005.5:c.2301C>A	ENSP00000316605.5:p.Pro767=
ENST00000517327.5:c.276+2756C>A	ENSP00000428329.1:n.276+2756C>A
NM_019098.4:c.2301C>A	NP_061971.3:p.Pro767=
XM_011517138.1:c.1887C>A	XP_011515440.1:p.Pro629=
XM_011517138.2:c.1887C>A	XP_011515440.1:p.Pro629=
NM_019098.5:c.2301C>A MANE Select	NP_061971.3:p.Pro767=