Canonical Allele Identifier: CA371447952
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86579201-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579201G>T , CM000670.2:g.86579201G>T GRCh38
NC_000008.10:g.87591429G>T , CM000670.1:g.87591429G>T GRCh37
NC_000008.9:g.87660545G>T NCBI36
NG_016980.1:g.169475C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1833C>A MANE Select ENSP00000316605.5:p.His611Gln
ENST00000681546.1:n.1653C>A
ENST00000681746.1:c.*244C>A ENSP00000505959.1:n.*244C>A
ENST00000320005.5:c.1833C>A ENSP00000316605.5:p.His611Gln
ENST00000517327.5:c.6C>A ENSP00000428329.1:p.His2Gln
NM_019098.4:c.1833C>A NP_061971.3:p.His611Gln
XM_011517138.1:c.1419C>A XP_011515440.1:p.His473Gln
XM_011517138.2:c.1419C>A XP_011515440.1:p.His473Gln
NM_019098.5:c.1833C>A MANE Select NP_061971.3:p.His611Gln