Canonical Allele Identifier: CA2687827911
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86739620-G-GGTT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739620_86739621insGTT , CM000670.2:g.86739620_86739621insGTT GRCh38
NC_000008.10:g.87751848_87751849insGTT , CM000670.1:g.87751848_87751849insGTT GRCh37
NC_000008.9:g.87820964_87820965insGTT NCBI36
NG_016980.1:g.9055_9056insAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.211+34_211+35insAAC MANE Select ENSP00000316605.5:n.211+34_211+35insAAC
ENST00000681746.1:c.211+34_211+35insAAC ENSP00000505959.1:n.211+34_211+35insAAC
ENST00000320005.5:c.211+34_211+35insAAC ENSP00000316605.5:n.211+34_211+35insAAC
ENST00000519777.1:n.193+34_193+35insAAC
NM_019098.4:c.211+34_211+35insAAC NP_061971.3:n.211+34_211+35insAAC
NM_019098.5:c.211+34_211+35insAAC MANE Select NP_061971.3:n.211+34_211+35insAAC
Search 100 bp 5'
Search 100 bp 3'