Canonical Allele Identifier: CA2669054007
Gene: CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190387938-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387938G>T , CM000665.2:g.190387938G>T GRCh38
NC_000003.11:g.190105727G>T , CM000665.1:g.190105727G>T GRCh37
NC_000003.10:g.191588421G>T NCBI36
NG_008149.1:g.4887G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-182G>T ENSP00000264734.2:n.-182G>T
ENST00000468220.1:n.306+13335G>T
NM_006580.3:c.-182G>T NP_006571.1:n.-182G>T
NM_001378492.1:c.-93-299G>T NP_001365421.1:n.-93-299G>T
NM_001378493.1:c.-93-299G>T NP_001365422.1:n.-93-299G>T
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