Canonical Allele Identifier: CA2753675
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs200322099
ExAC: 3:190105906 A / G
gnomAD v2: 3-190105906-A-G
gnomAD v4: 3-190388117-A-G
MyVariant Identifiers: chr3:g.190105906A>G (hg19) chr3:g.190388117A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388117A>G , CM000665.2:g.190388117A>G GRCh38
NC_000003.11:g.190105906A>G , CM000665.1:g.190105906A>G GRCh37
NC_000003.10:g.191588600A>G NCBI36
NG_008149.1:g.5066A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-3A>G ENSP00000264734.2:n.-3A>G
ENST00000468220.1:n.306+13514A>G
NM_006580.3:c.-3A>G NP_006571.1:n.-3A>G
NM_001378492.1:c.-93-120A>G NP_001365421.1:n.-93-120A>G
NM_001378493.1:c.-93-120A>G NP_001365422.1:n.-93-120A>G
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