Canonical Allele Identifier: CA437637074
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190105947G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388158G>A , CM000665.2:g.190388158G>A GRCh38
NC_000003.11:g.190105947G>A , CM000665.1:g.190105947G>A GRCh37
NC_000003.10:g.191588641G>A NCBI36
NG_008149.1:g.5107G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456423.2:c.-172G>A ENSP00000414136.2:n.-172G>A
ENST00000264734.2:c.39G>A ENSP00000264734.2:p.Leu13=
ENST00000456423.1:c.39G>A ENSP00000414136.1:p.Leu13=
ENST00000468220.1:n.306+13555G>A
NM_006580.3:c.39G>A NP_006571.1:p.Leu13=
NM_001378492.1:c.-93-79G>A NP_001365421.1:n.-93-79G>A
NM_001378493.1:c.-93-79G>A NP_001365422.1:n.-93-79G>A
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