Canonical Allele Identifier: CA548494047
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs768547943
gnomAD v2: 3-190105867-G-T
gnomAD v4: 3-190388078-G-T
MyVariant Identifiers: chr3:g.190105867G>T (hg19) chr3:g.190388078G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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