Canonical Allele Identifier: CA371448298
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86647878-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647878C>A , CM000670.2:g.86647878C>A GRCh38
NC_000008.10:g.87660106C>A , CM000670.1:g.87660106C>A GRCh37
NC_000008.9:g.87729222C>A NCBI36
NG_016980.1:g.100798G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.913G>T MANE Select ENSP00000316605.5:p.Ala305Ser
ENST00000681546.1:n.733G>T
ENST00000681746.1:c.913G>T ENSP00000505959.1:p.Ala305Ser
ENST00000320005.5:c.913G>T ENSP00000316605.5:p.Ala305Ser
NM_019098.4:c.913G>T NP_061971.3:p.Ala305Ser
XM_011517138.1:c.499G>T XP_011515440.1:p.Ala167Ser
XM_011517138.2:c.499G>T XP_011515440.1:p.Ala167Ser
NM_019098.5:c.913G>T MANE Select NP_061971.3:p.Ala305Ser