Canonical Allele Identifier: CA2687823102
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86574106-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86574106T>A , CM000670.2:g.86574106T>A GRCh38
NC_000008.10:g.87586334T>A , CM000670.1:g.87586334T>A GRCh37
NC_000008.9:g.87655450T>A NCBI36
NG_016980.1:g.174570A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000681746.1:c.*2539A>T ENSP00000505959.1:n.*2539A>T
ENST00000320005.5:c.*1698A>T ENSP00000316605.5:n.*1698A>T
ENST00000517327.5:c.276+4583A>T ENSP00000428329.1:n.276+4583A>T
NM_019098.4:c.*1698A>T NP_061971.3:n.*1698A>T
XM_011517138.1:c.*1698A>T XP_011515440.1:n.*1698A>T
XM_011517138.2:c.*1698A>T XP_011515440.1:n.*1698A>T