Canonical Allele Identifier: CA371456779
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86739721-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739721C>A , CM000670.2:g.86739721C>A GRCh38
NC_000008.10:g.87751949C>A , CM000670.1:g.87751949C>A GRCh37
NC_000008.9:g.87821065C>A NCBI36
NG_016980.1:g.8955G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.145G>T MANE Select ENSP00000316605.5:p.Glu49Ter
ENST00000681746.1:c.145G>T ENSP00000505959.1:p.Glu49Ter
ENST00000320005.5:c.145G>T ENSP00000316605.5:p.Glu49Ter
ENST00000519777.1:n.127G>T
NM_019098.4:c.145G>T NP_061971.3:p.Glu49Ter
NM_019098.5:c.145G>T MANE Select NP_061971.3:p.Glu49Ter