Canonical Allele Identifier: CA371456749
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86739709-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739709G>T , CM000670.2:g.86739709G>T GRCh38
NC_000008.10:g.87751937G>T , CM000670.1:g.87751937G>T GRCh37
NC_000008.9:g.87821053G>T NCBI36
NG_016980.1:g.8967C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.157C>A MANE Select ENSP00000316605.5:p.Leu53Ile
ENST00000681746.1:c.157C>A ENSP00000505959.1:p.Leu53Ile
ENST00000320005.5:c.157C>A ENSP00000316605.5:p.Leu53Ile
ENST00000519777.1:n.139C>A
NM_019098.4:c.157C>A NP_061971.3:p.Leu53Ile
NM_019098.5:c.157C>A MANE Select NP_061971.3:p.Leu53Ile