Canonical Allele Identifier: CA371448307
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86647882-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647882A>T , CM000670.2:g.86647882A>T GRCh38
NC_000008.10:g.87660110A>T , CM000670.1:g.87660110A>T GRCh37
NC_000008.9:g.87729226A>T NCBI36
NG_016980.1:g.100794T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.909T>A MANE Select ENSP00000316605.5:p.Asp303Glu
ENST00000681546.1:n.729T>A
ENST00000681746.1:c.909T>A ENSP00000505959.1:p.Asp303Glu
ENST00000320005.5:c.909T>A ENSP00000316605.5:p.Asp303Glu
NM_019098.4:c.909T>A NP_061971.3:p.Asp303Glu
XM_011517138.1:c.495T>A XP_011515440.1:p.Asp165Glu
XM_011517138.2:c.495T>A XP_011515440.1:p.Asp165Glu
NM_019098.5:c.909T>A MANE Select NP_061971.3:p.Asp303Glu