Canonical Allele Identifier: CA371448309
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1369514767
gnomAD v2: 8-87660111-T-C
gnomAD v4: 8-86647883-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647883T>C , CM000670.2:g.86647883T>C GRCh38
NC_000008.10:g.87660111T>C , CM000670.1:g.87660111T>C GRCh37
NC_000008.9:g.87729227T>C NCBI36
NG_016980.1:g.100793A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.908A>G MANE Select ENSP00000316605.5:p.Asp303Gly
ENST00000681546.1:n.728A>G
ENST00000681746.1:c.908A>G ENSP00000505959.1:p.Asp303Gly
ENST00000320005.5:c.908A>G ENSP00000316605.5:p.Asp303Gly
NM_019098.4:c.908A>G NP_061971.3:p.Asp303Gly
XM_011517138.1:c.494A>G XP_011515440.1:p.Asp165Gly
XM_011517138.2:c.494A>G XP_011515440.1:p.Asp165Gly
NM_019098.5:c.908A>G MANE Select NP_061971.3:p.Asp303Gly