Canonical Allele Identifier: CA461816403

Gene: CNGB3

Linked Data

• dbSNP Id: rs1159739100
• gnomAD v4: 8-86647887-A-G
• MyVariant Identifiers: chr8:g.87660115A>G (hg19) ; chr8:g.86647887A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86647887A>G , CM000670.2:g.86647887A>G	GRCh38
NC_000008.10:g.87660115A>G , CM000670.1:g.87660115A>G	GRCh37
NC_000008.9:g.87729231A>G	NCBI36
NG_016980.1:g.100789T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.904T>C MANE Select	ENSP00000316605.5:p.Leu302=
ENST00000681546.1:n.724T>C
ENST00000681746.1:c.904T>C	ENSP00000505959.1:p.Leu302=
ENST00000320005.5:c.904T>C	ENSP00000316605.5:p.Leu302=
NM_019098.4:c.904T>C	NP_061971.3:p.Leu302=
XM_011517138.1:c.490T>C	XP_011515440.1:p.Leu164=
XM_011517138.2:c.490T>C	XP_011515440.1:p.Leu164=
NM_019098.5:c.904T>C MANE Select	NP_061971.3:p.Leu302=