Canonical Allele Identifier: CA371447956
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86579203-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579203G>A , CM000670.2:g.86579203G>A GRCh38
NC_000008.10:g.87591431G>A , CM000670.1:g.87591431G>A GRCh37
NC_000008.9:g.87660547G>A NCBI36
NG_016980.1:g.169473C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1831C>T MANE Select ENSP00000316605.5:p.His611Tyr
ENST00000681546.1:n.1651C>T
ENST00000681746.1:c.*242C>T ENSP00000505959.1:n.*242C>T
ENST00000320005.5:c.1831C>T ENSP00000316605.5:p.His611Tyr
ENST00000517327.5:c.4C>T ENSP00000428329.1:p.His2Tyr
NM_019098.4:c.1831C>T NP_061971.3:p.His611Tyr
XM_011517138.1:c.1417C>T XP_011515440.1:p.His473Tyr
XM_011517138.2:c.1417C>T XP_011515440.1:p.His473Tyr
NM_019098.5:c.1831C>T MANE Select NP_061971.3:p.His611Tyr