Canonical Allele Identifier: CA2588340557
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739620_86739621delinsGT , CM000670.2:g.86739620_86739621delinsGT GRCh38
NC_000008.10:g.87751848_87751849delinsGT , CM000670.1:g.87751848_87751849delinsGT GRCh37
NC_000008.9:g.87820964_87820965delinsGT NCBI36
NG_016980.1:g.9055_9056delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.211+34_211+35delinsAC MANE Select ENSP00000316605.5:n.211+34_211+35delinsAC...
ENST00000681746.1:c.211+34_211+35delinsAC ENSP00000505959.1:n.211+34_211+35delinsAC...
ENST00000320005.5:c.211+34_211+35delinsAC ENSP00000316605.5:n.211+34_211+35delinsAC...
ENST00000519777.1:n.193+34_193+35delinsAC
NM_019098.4:c.211+34_211+35delinsAC NP_061971.3:n.211+34_211+35delinsAC
NM_019098.5:c.211+34_211+35delinsAC MANE Select NP_061971.3:n.211+34_211+35delinsAC