Canonical Allele Identifier: CA1428775446
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1718548121
gnomAD v4: 3-190388008-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388008C>T , CM000665.2:g.190388008C>T GRCh38
NC_000003.11:g.190105797C>T , CM000665.1:g.190105797C>T GRCh37
NC_000003.10:g.191588491C>T NCBI36
NG_008149.1:g.4957C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-112C>T ENSP00000264734.2:n.-112C>T
ENST00000468220.1:n.306+13405C>T
NM_006580.3:c.-112C>T NP_006571.1:n.-112C>T
NM_001378492.1:c.-93-229C>T NP_001365421.1:n.-93-229C>T
NM_001378493.1:c.-93-229C>T NP_001365422.1:n.-93-229C>T
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