Canonical Allele Identifier: CA2687825557
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647776del , CM000670.2:g.86647776del GRCh38
NC_000008.10:g.87660004del , CM000670.1:g.87660004del GRCh37
NC_000008.9:g.87729120del NCBI36
NG_016980.1:g.100903del

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.990+28del MANE Select ENSP00000316605.5:n.990+28del
ENST00000681546.1:n.810+28del
ENST00000681746.1:c.990+28del ENSP00000505959.1:n.990+28del
ENST00000320005.5:c.990+28del ENSP00000316605.5:n.990+28del
NM_019098.4:c.990+28del NP_061971.3:n.990+28del
XM_011517138.1:c.576+28del XP_011515440.1:n.576+28del
XM_011517138.2:c.576+28del XP_011515440.1:n.576+28del
NM_019098.5:c.990+28del MANE Select NP_061971.3:n.990+28del