Canonical Allele Identifier: CA1428775507
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1577421084
gnomAD v4: 3-190388080-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388080A>C , CM000665.2:g.190388080A>C GRCh38
NC_000003.11:g.190105869A>C , CM000665.1:g.190105869A>C GRCh37
NC_000003.10:g.191588563A>C NCBI36
NG_008149.1:g.5029A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-40A>C ENSP00000264734.2:n.-40A>C
ENST00000468220.1:n.306+13477A>C
NM_006580.3:c.-40A>C NP_006571.1:n.-40A>C
NM_001378492.1:c.-93-157A>C NP_001365421.1:n.-93-157A>C
NM_001378493.1:c.-93-157A>C NP_001365422.1:n.-93-157A>C
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