Canonical Allele Identifier: CA371448323

Gene: CNGB3

Linked Data

• MyVariant Identifiers: chr8:g.87660116C>G (hg19) ; chr8:g.86647888C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86647888C>G , CM000670.2:g.86647888C>G	GRCh38
NC_000008.10:g.87660116C>G , CM000670.1:g.87660116C>G	GRCh37
NC_000008.9:g.87729232C>G	NCBI36
NG_016980.1:g.100788G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.904-1G>C MANE Select	ENSP00000316605.5:n.904-1G>C
ENST00000681546.1:n.724-1G>C
ENST00000681746.1:c.904-1G>C	ENSP00000505959.1:n.904-1G>C
ENST00000320005.5:c.904-1G>C	ENSP00000316605.5:n.904-1G>C
NM_019098.4:c.904-1G>C	NP_061971.3:n.904-1G>C
XM_011517138.1:c.490-1G>C	XP_011515440.1:n.490-1G>C
XM_011517138.2:c.490-1G>C	XP_011515440.1:n.490-1G>C
NM_019098.5:c.904-1G>C MANE Select	NP_061971.3:n.904-1G>C