Canonical Allele Identifier: CA904279012
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1365257989
gnomAD v3: 3-190387989-C-G
gnomAD v4: 3-190387989-C-G
MyVariant Identifiers: chr3:g.190105778C>G (hg19) chr3:g.190387989C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387989C>G , CM000665.2:g.190387989C>G GRCh38
NC_000003.11:g.190105778C>G , CM000665.1:g.190105778C>G GRCh37
NC_000003.10:g.191588472C>G NCBI36
NG_008149.1:g.4938C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-131C>G ENSP00000264734.2:n.-131C>G
ENST00000468220.1:n.306+13386C>G
NM_006580.3:c.-131C>G NP_006571.1:n.-131C>G
NM_001378492.1:c.-93-248C>G NP_001365421.1:n.-93-248C>G
NM_001378493.1:c.-93-248C>G NP_001365422.1:n.-93-248C>G
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