Canonical Allele Identifier: CA2687827863
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86739618-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739618T>C , CM000670.2:g.86739618T>C GRCh38
NC_000008.10:g.87751846T>C , CM000670.1:g.87751846T>C GRCh37
NC_000008.9:g.87820962T>C NCBI36
NG_016980.1:g.9058A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.211+37A>G MANE Select ENSP00000316605.5:n.211+37A>G
ENST00000681746.1:c.211+37A>G ENSP00000505959.1:n.211+37A>G
ENST00000320005.5:c.211+37A>G ENSP00000316605.5:n.211+37A>G
ENST00000519777.1:n.193+37A>G
NM_019098.4:c.211+37A>G NP_061971.3:n.211+37A>G
NM_019098.5:c.211+37A>G MANE Select NP_061971.3:n.211+37A>G