Canonical Allele Identifier: CA2781158514
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739916_86739920del , CM000670.2:g.86739916_86739920del GRCh38
NC_000008.10:g.87752144_87752148del , CM000670.1:g.87752144_87752148del GRCh37
NC_000008.9:g.87821260_87821264del NCBI36
NG_016980.1:g.8756_8760del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.130-184_130-180del MANE Select ENSP00000316605.5:n.130-184_130-180del
ENST00000681746.1:c.130-184_130-180del ENSP00000505959.1:n.130-184_130-180del
ENST00000320005.5:c.130-184_130-180del ENSP00000316605.5:n.130-184_130-180del
ENST00000519777.1:n.112-184_112-180del
NM_019098.4:c.130-184_130-180del NP_061971.3:n.130-184_130-180del
NM_019098.5:c.130-184_130-180del MANE Select NP_061971.3:n.130-184_130-180del