Canonical Allele Identifier: CA461816107
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86647806-A-G
MyVariant Identifiers: chr8:g.87660034A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647806A>G , CM000670.2:g.86647806A>G GRCh38
NC_000008.10:g.87660034A>G , CM000670.1:g.87660034A>G GRCh37
NC_000008.9:g.87729150A>G NCBI36
NG_016980.1:g.100870T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.985T>C MANE Select ENSP00000316605.5:p.Leu329=
ENST00000681546.1:n.805T>C
ENST00000681746.1:c.985T>C ENSP00000505959.1:p.Leu329=
ENST00000320005.5:c.985T>C ENSP00000316605.5:p.Leu329=
NM_019098.4:c.985T>C NP_061971.3:p.Leu329=
XM_011517138.1:c.571T>C XP_011515440.1:p.Leu191=
XM_011517138.2:c.571T>C XP_011515440.1:p.Leu191=
NM_019098.5:c.985T>C MANE Select NP_061971.3:p.Leu329=