Canonical Allele Identifier: CA1116237175
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739619_86739620del , CM000670.2:g.86739619_86739620del GRCh38
NC_000008.10:g.87751847_87751848del , CM000670.1:g.87751847_87751848del GRCh37
NC_000008.9:g.87820963_87820964del NCBI36
NG_016980.1:g.9056_9057del

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.211+35_211+36del MANE Select ENSP00000316605.5:n.211+35_211+36del
ENST00000681746.1:c.211+35_211+36del ENSP00000505959.1:n.211+35_211+36del
ENST00000320005.5:c.211+35_211+36del ENSP00000316605.5:n.211+35_211+36del
ENST00000519777.1:n.193+35_193+36del
NM_019098.4:c.211+35_211+36del NP_061971.3:n.211+35_211+36del
NM_019098.5:c.211+35_211+36del MANE Select NP_061971.3:n.211+35_211+36del