Canonical Allele Identifier: CA371447976
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86579213-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579213A>C , CM000670.2:g.86579213A>C GRCh38
NC_000008.10:g.87591441A>C , CM000670.1:g.87591441A>C GRCh37
NC_000008.9:g.87660557A>C NCBI36
NG_016980.1:g.169463T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1821T>G MANE Select ENSP00000316605.5:p.Asn607Lys
ENST00000681546.1:n.1641T>G
ENST00000681746.1:c.*232T>G ENSP00000505959.1:n.*232T>G
ENST00000320005.5:c.1821T>G ENSP00000316605.5:p.Asn607Lys
NM_019098.4:c.1821T>G NP_061971.3:p.Asn607Lys
XM_011517138.1:c.1407T>G XP_011515440.1:p.Asn469Lys
XM_011517138.2:c.1407T>G XP_011515440.1:p.Asn469Lys
NM_019098.5:c.1821T>G MANE Select NP_061971.3:p.Asn607Lys