Canonical Allele Identifier: CA461831089
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86668032-T-G
MyVariant Identifiers: chr8:g.87680260T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668032T>G , CM000670.2:g.86668032T>G GRCh38
NC_000008.10:g.87680260T>G , CM000670.1:g.87680260T>G GRCh37
NC_000008.9:g.87749376T>G NCBI36
NG_016980.1:g.80644A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.630A>C MANE Select ENSP00000316605.5:p.Ile210=
ENST00000681746.1:c.630A>C ENSP00000505959.1:p.Ile210=
ENST00000320005.5:c.630A>C ENSP00000316605.5:p.Ile210=
NM_019098.4:c.630A>C NP_061971.3:p.Ile210=
XM_011517138.1:c.216A>C XP_011515440.1:p.Ile72=
XM_011517138.2:c.216A>C XP_011515440.1:p.Ile72=
NM_019098.5:c.630A>C MANE Select NP_061971.3:p.Ile210=