Canonical Allele Identifier: CA2669054112
Gene: CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190388059-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388059C>A , CM000665.2:g.190388059C>A GRCh38
NC_000003.11:g.190105848C>A , CM000665.1:g.190105848C>A GRCh37
NC_000003.10:g.191588542C>A NCBI36
NG_008149.1:g.5008C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-61C>A ENSP00000264734.2:n.-61C>A
ENST00000468220.1:n.306+13456C>A
NM_006580.3:c.-61C>A NP_006571.1:n.-61C>A
NM_001378492.1:c.-93-178C>A NP_001365421.1:n.-93-178C>A
NM_001378493.1:c.-93-178C>A NP_001365422.1:n.-93-178C>A
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