Canonical Allele Identifier: CA1116219122
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671220_86671225del , CM000670.2:g.86671220_86671225del GRCh38
NC_000008.10:g.87683448_87683453del , CM000670.1:g.87683448_87683453del GRCh37
NC_000008.9:g.87752564_87752569del NCBI36
NG_016980.1:g.77451_77456del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.339-127_339-122del MANE Select ENSP00000316605.5:n.339-127_339-122del
ENST00000680314.1:n.100-127_100-122del
ENST00000681746.1:c.339-127_339-122del ENSP00000505959.1:n.339-127_339-122del
ENST00000320005.5:c.339-127_339-122del ENSP00000316605.5:n.339-127_339-122del
NM_019098.4:c.339-127_339-122del NP_061971.3:n.339-127_339-122del
XM_011517138.1:c.-76-127_-76-122del XP_011515440.1:n.-76-127_-76-122del
XM_011517138.2:c.-76-127_-76-122del XP_011515440.1:n.-76-127_-76-122del
NM_019098.5:c.339-127_339-122del MANE Select NP_061971.3:n.339-127_339-122del