Canonical Allele Identifier: CA548494025
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1243141472
gnomAD v2: 3-190105741-T-A
gnomAD v3: 3-190387952-T-A
gnomAD v4: 3-190387952-T-A
MyVariant Identifiers: chr3:g.190105741T>A (hg19) chr3:g.190387952T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387952T>A , CM000665.2:g.190387952T>A GRCh38
NC_000003.11:g.190105741T>A , CM000665.1:g.190105741T>A GRCh37
NC_000003.10:g.191588435T>A NCBI36
NG_008149.1:g.4901T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-168T>A ENSP00000264734.2:n.-168T>A
ENST00000468220.1:n.306+13349T>A
NM_006580.3:c.-168T>A NP_006571.1:n.-168T>A
NM_001378492.1:c.-93-285T>A NP_001365421.1:n.-93-285T>A
NM_001378493.1:c.-93-285T>A NP_001365422.1:n.-93-285T>A
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