Canonical Allele Identifier: CA371449702
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86668024-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668024T>C , CM000670.2:g.86668024T>C GRCh38
NC_000008.10:g.87680252T>C , CM000670.1:g.87680252T>C GRCh37
NC_000008.9:g.87749368T>C NCBI36
NG_016980.1:g.80652A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.638A>G MANE Select ENSP00000316605.5:p.Tyr213Cys
ENST00000681746.1:c.638A>G ENSP00000505959.1:p.Tyr213Cys
ENST00000320005.5:c.638A>G ENSP00000316605.5:p.Tyr213Cys
NM_019098.4:c.638A>G NP_061971.3:p.Tyr213Cys
XM_011517138.1:c.224A>G XP_011515440.1:p.Tyr75Cys
XM_011517138.2:c.224A>G XP_011515440.1:p.Tyr75Cys
NM_019098.5:c.638A>G MANE Select NP_061971.3:p.Tyr213Cys