Canonical Allele Identifier: CA2669054085
Gene: CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190388018-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388018G>A , CM000665.2:g.190388018G>A GRCh38
NC_000003.11:g.190105807G>A , CM000665.1:g.190105807G>A GRCh37
NC_000003.10:g.191588501G>A NCBI36
NG_008149.1:g.4967G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-102G>A ENSP00000264734.2:n.-102G>A
ENST00000468220.1:n.306+13415G>A
NM_006580.3:c.-102G>A NP_006571.1:n.-102G>A
NM_001378492.1:c.-93-219G>A NP_001365421.1:n.-93-219G>A
NM_001378493.1:c.-93-219G>A NP_001365422.1:n.-93-219G>A
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