Canonical Allele Identifier: CA89749519
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1014212525

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387959C>T , CM000665.2:g.190387959C>T GRCh38
NC_000003.11:g.190105748C>T , CM000665.1:g.190105748C>T GRCh37
NC_000003.10:g.191588442C>T NCBI36
NG_008149.1:g.4908C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-161C>T ENSP00000264734.2:n.-161C>T
ENST00000468220.1:n.306+13356C>T
NM_006580.3:c.-161C>T NP_006571.1:n.-161C>T
NM_001378492.1:c.-93-278C>T NP_001365421.1:n.-93-278C>T
NM_001378493.1:c.-93-278C>T NP_001365422.1:n.-93-278C>T