Canonical Allele Identifier: CA548798497
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1284499114
gnomAD v2: 3-190105902-T-C
gnomAD v4: 3-190388113-T-C
MyVariant Identifiers: chr3:g.190105902T>C (hg19) chr3:g.190388113T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388113T>C , CM000665.2:g.190388113T>C GRCh38
NC_000003.11:g.190105902T>C , CM000665.1:g.190105902T>C GRCh37
NC_000003.10:g.191588596T>C NCBI36
NG_008149.1:g.5062T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-7T>C ENSP00000264734.2:n.-7T>C
ENST00000468220.1:n.306+13510T>C
NM_006580.3:c.-7T>C NP_006571.1:n.-7T>C
NM_001378492.1:c.-93-124T>C NP_001365421.1:n.-93-124T>C
NM_001378493.1:c.-93-124T>C NP_001365422.1:n.-93-124T>C
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