Canonical Allele Identifier: CA2753664
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs768547943
ExAC: 3:190105867 G / A
gnomAD v2: 3-190105867-G-A
MyVariant Identifiers: chr3:g.190105867G>A (hg19) chr3:g.190388078G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388078G>A , CM000665.2:g.190388078G>A GRCh38
NC_000003.11:g.190105867G>A , CM000665.1:g.190105867G>A GRCh37
NC_000003.10:g.191588561G>A NCBI36
NG_008149.1:g.5027G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-42G>A ENSP00000264734.2:n.-42G>A
ENST00000468220.1:n.306+13475G>A
NM_006580.3:c.-42G>A NP_006571.1:n.-42G>A
NM_001378492.1:c.-93-159G>A NP_001365421.1:n.-93-159G>A
NM_001378493.1:c.-93-159G>A NP_001365422.1:n.-93-159G>A
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