Canonical Allele Identifier: CA371449699
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668023G>C , CM000670.2:g.86668023G>C GRCh38
NC_000008.10:g.87680251G>C , CM000670.1:g.87680251G>C GRCh37
NC_000008.9:g.87749367G>C NCBI36
NG_016980.1:g.80653C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.639C>G MANE Select ENSP00000316605.5:p.Tyr213Ter
ENST00000681746.1:c.639C>G ENSP00000505959.1:p.Tyr213Ter
ENST00000320005.5:c.639C>G ENSP00000316605.5:p.Tyr213Ter
NM_019098.4:c.639C>G NP_061971.3:p.Tyr213Ter
XM_011517138.1:c.225C>G XP_011515440.1:p.Tyr75Ter
XM_011517138.2:c.225C>G XP_011515440.1:p.Tyr75Ter
NM_019098.5:c.639C>G MANE Select NP_061971.3:p.Tyr213Ter