Canonical Allele Identifier: CA2669053994
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387924A>G , CM000665.2:g.190387924A>G GRCh38
NC_000003.11:g.190105713A>G , CM000665.1:g.190105713A>G GRCh37
NC_000003.10:g.191588407A>G NCBI36
NG_008149.1:g.4873A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-196A>G ENSP00000264734.2:n.-196A>G
ENST00000468220.1:n.306+13321A>G
NM_006580.3:c.-196A>G NP_006571.1:n.-196A>G
NM_001378492.1:c.-93-313A>G NP_001365421.1:n.-93-313A>G
NM_001378493.1:c.-93-313A>G NP_001365422.1:n.-93-313A>G