Canonical Allele Identifier: CA904279027
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1456776139

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388032C>T , CM000665.2:g.190388032C>T GRCh38
NC_000003.11:g.190105821C>T , CM000665.1:g.190105821C>T GRCh37
NC_000003.10:g.191588515C>T NCBI36
NG_008149.1:g.4981C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-88C>T ENSP00000264734.2:n.-88C>T
ENST00000468220.1:n.306+13429C>T
NM_006580.3:c.-88C>T NP_006571.1:n.-88C>T
NM_001378492.1:c.-93-205C>T NP_001365421.1:n.-93-205C>T
NM_001378493.1:c.-93-205C>T NP_001365422.1:n.-93-205C>T