Canonical Allele Identifier: CA461816089
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86647801-C-T
MyVariant Identifiers: chr8:g.87660029C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647801C>T , CM000670.2:g.86647801C>T GRCh38
NC_000008.10:g.87660029C>T , CM000670.1:g.87660029C>T GRCh37
NC_000008.9:g.87729145C>T NCBI36
NG_016980.1:g.100875G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.990G>A MANE Select ENSP00000316605.5:p.Lys330=
ENST00000681546.1:n.810G>A
ENST00000681746.1:c.990G>A ENSP00000505959.1:p.Lys330=
ENST00000320005.5:c.990G>A ENSP00000316605.5:p.Lys330=
NM_019098.4:c.990G>A NP_061971.3:p.Lys330=
XM_011517138.1:c.576G>A XP_011515440.1:p.Lys192=
XM_011517138.2:c.576G>A XP_011515440.1:p.Lys192=
NM_019098.5:c.990G>A MANE Select NP_061971.3:p.Lys330=