Canonical Allele Identifier: CA371448297
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86647877-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647877G>T , CM000670.2:g.86647877G>T GRCh38
NC_000008.10:g.87660105G>T , CM000670.1:g.87660105G>T GRCh37
NC_000008.9:g.87729221G>T NCBI36
NG_016980.1:g.100799C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.914C>A MANE Select ENSP00000316605.5:p.Ala305Glu
ENST00000681546.1:n.734C>A
ENST00000681746.1:c.914C>A ENSP00000505959.1:p.Ala305Glu
ENST00000320005.5:c.914C>A ENSP00000316605.5:p.Ala305Glu
NM_019098.4:c.914C>A NP_061971.3:p.Ala305Glu
XM_011517138.1:c.500C>A XP_011515440.1:p.Ala167Glu
XM_011517138.2:c.500C>A XP_011515440.1:p.Ala167Glu
NM_019098.5:c.914C>A MANE Select NP_061971.3:p.Ala305Glu