Canonical Allele Identifier: CA2669054114
Gene: CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190388063-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388063A>C , CM000665.2:g.190388063A>C GRCh38
NC_000003.11:g.190105852A>C , CM000665.1:g.190105852A>C GRCh37
NC_000003.10:g.191588546A>C NCBI36
NG_008149.1:g.5012A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-57A>C ENSP00000264734.2:n.-57A>C
ENST00000468220.1:n.306+13460A>C
NM_006580.3:c.-57A>C NP_006571.1:n.-57A>C
NM_001378492.1:c.-93-174A>C NP_001365421.1:n.-93-174A>C
NM_001378493.1:c.-93-174A>C NP_001365422.1:n.-93-174A>C
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