Canonical Allele Identifier: CA371449893
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1370084296
gnomAD v4: 8-86668111-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668111T>C , CM000670.2:g.86668111T>C GRCh38
NC_000008.10:g.87680339T>C , CM000670.1:g.87680339T>C GRCh37
NC_000008.9:g.87749455T>C NCBI36
NG_016980.1:g.80565A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.551A>G MANE Select ENSP00000316605.5:p.Tyr184Cys
ENST00000681746.1:c.551A>G ENSP00000505959.1:p.Tyr184Cys
ENST00000320005.5:c.551A>G ENSP00000316605.5:p.Tyr184Cys
NM_019098.4:c.551A>G NP_061971.3:p.Tyr184Cys
XM_011517138.1:c.137A>G XP_011515440.1:p.Tyr46Cys
XM_011517138.2:c.137A>G XP_011515440.1:p.Tyr46Cys
NM_019098.5:c.551A>G MANE Select NP_061971.3:p.Tyr184Cys