Canonical Allele Identifier: CA2781158481
Gene: CNGB3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739876del , CM000670.2:g.86739876del GRCh38
NC_000008.10:g.87752104del , CM000670.1:g.87752104del GRCh37
NC_000008.9:g.87821220del NCBI36
NG_016980.1:g.8801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.130-139del MANE Select ENSP00000316605.5:n.130-139del
ENST00000681746.1:c.130-139del ENSP00000505959.1:n.130-139del
ENST00000320005.5:c.130-139del ENSP00000316605.5:n.130-139del
ENST00000519777.1:n.112-139del
NM_019098.4:c.130-139del NP_061971.3:n.130-139del
NM_019098.5:c.130-139del MANE Select NP_061971.3:n.130-139del
Search 100 bp 5'
Search 100 bp 3'