Canonical Allele Identifier: CA2687827882
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739638_86739639insTTTTTGTTTTTTTTTTTTTTTTTTTTTT , CM000670.2:g.86739638_86739639insTTTTTGTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000008.10:g.87751866_87751867insTTTTTGTTTTTTTTTTTTTTTTTTTTTT , CM000670.1:g.87751866_87751867insTTTTTGTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000008.9:g.87820982_87820983insTTTTTGTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_016980.1:g.9055_9056insAAAACAAAAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

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