Canonical Allele Identifier: CA461816359
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86647876-T-C
MyVariant Identifiers: chr8:g.87660104T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647876T>C , CM000670.2:g.86647876T>C GRCh38
NC_000008.10:g.87660104T>C , CM000670.1:g.87660104T>C GRCh37
NC_000008.9:g.87729220T>C NCBI36
NG_016980.1:g.100800A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.915A>G MANE Select ENSP00000316605.5:p.Ala305=
ENST00000681546.1:n.735A>G
ENST00000681746.1:c.915A>G ENSP00000505959.1:p.Ala305=
ENST00000320005.5:c.915A>G ENSP00000316605.5:p.Ala305=
NM_019098.4:c.915A>G NP_061971.3:p.Ala305=
XM_011517138.1:c.501A>G XP_011515440.1:p.Ala167=
XM_011517138.2:c.501A>G XP_011515440.1:p.Ala167=
NM_019098.5:c.915A>G MANE Select NP_061971.3:p.Ala305=