Canonical Allele Identifier: CA89749517
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs552441627
gnomAD v3: 3-190387941-C-G
gnomAD v4: 3-190387941-C-G
MyVariant Identifiers: chr3:g.190105730C>G (hg19) chr3:g.190387941C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387941C>G , CM000665.2:g.190387941C>G GRCh38
NC_000003.11:g.190105730C>G , CM000665.1:g.190105730C>G GRCh37
NC_000003.10:g.191588424C>G NCBI36
NG_008149.1:g.4890C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-179C>G ENSP00000264734.2:n.-179C>G
ENST00000468220.1:n.306+13338C>G
NM_006580.3:c.-179C>G NP_006571.1:n.-179C>G
NM_001378492.1:c.-93-296C>G NP_001365421.1:n.-93-296C>G
NM_001378493.1:c.-93-296C>G NP_001365422.1:n.-93-296C>G
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