Canonical Allele Identifier: CA2687827003
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86667156-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86667156A>C , CM000670.2:g.86667156A>C GRCh38
NC_000008.10:g.87679384A>C , CM000670.1:g.87679384A>C GRCh37
NC_000008.9:g.87748500A>C NCBI36
NG_016980.1:g.81520T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.644-23T>G MANE Select ENSP00000316605.5:n.644-23T>G
ENST00000681746.1:c.644-23T>G ENSP00000505959.1:n.644-23T>G
ENST00000320005.5:c.644-23T>G ENSP00000316605.5:n.644-23T>G
NM_019098.4:c.644-23T>G NP_061971.3:n.644-23T>G
XM_011517138.1:c.230-23T>G XP_011515440.1:n.230-23T>G
XM_011517138.2:c.230-23T>G XP_011515440.1:n.230-23T>G
NM_019098.5:c.644-23T>G MANE Select NP_061971.3:n.644-23T>G