Canonical Allele Identifier: CA461813700

Gene: CNGB3

Linked Data

• MyVariant Identifiers: chr8:g.87644980C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86632752C>T , CM000670.2:g.86632752C>T	GRCh38
NC_000008.10:g.87644980C>T , CM000670.1:g.87644980C>T	GRCh37
NC_000008.9:g.87714096C>T	NCBI36
NG_016980.1:g.115924G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.1320G>A MANE Select	ENSP00000316605.5:p.Gln440=
ENST00000681546.1:n.1140G>A
ENST00000681746.1:c.1320G>A	ENSP00000505959.1:p.Gln440=
ENST00000320005.5:c.1320G>A	ENSP00000316605.5:p.Gln440=
NM_019098.4:c.1320G>A	NP_061971.3:p.Gln440=
XM_011517138.1:c.906G>A	XP_011515440.1:p.Gln302=
XM_011517138.2:c.906G>A	XP_011515440.1:p.Gln302=
NM_019098.5:c.1320G>A MANE Select	NP_061971.3:p.Gln440=