Canonical Allele Identifier: CA2669054142
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs2108657992
gnomAD v4: 3-190388119-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388119A>G , CM000665.2:g.190388119A>G GRCh38
NC_000003.11:g.190105908A>G , CM000665.1:g.190105908A>G GRCh37
NC_000003.10:g.191588602A>G NCBI36
NG_008149.1:g.5068A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-1A>G ENSP00000264734.2:n.-1A>G
ENST00000468220.1:n.306+13516A>G
NM_006580.3:c.-1A>G NP_006571.1:n.-1A>G
NM_001378492.1:c.-93-118A>G NP_001365421.1:n.-93-118A>G
NM_001378493.1:c.-93-118A>G NP_001365422.1:n.-93-118A>G
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