Canonical Allele Identifier: CA89749516
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs960371235
gnomAD v2: 3-190105710-G-C
gnomAD v3: 3-190387921-G-C
gnomAD v4: 3-190387921-G-C
MyVariant Identifiers: chr3:g.190105710G>C (hg19) chr3:g.190387921G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387921G>C , CM000665.2:g.190387921G>C GRCh38
NC_000003.11:g.190105710G>C , CM000665.1:g.190105710G>C GRCh37
NC_000003.10:g.191588404G>C NCBI36
NG_008149.1:g.4870G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-199G>C ENSP00000264734.2:n.-199G>C
ENST00000468220.1:n.306+13318G>C
NM_006580.3:c.-199G>C NP_006571.1:n.-199G>C
NM_001378492.1:c.-93-316G>C NP_001365421.1:n.-93-316G>C
NM_001378493.1:c.-93-316G>C NP_001365422.1:n.-93-316G>C
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