Canonical Allele Identifier: CA2554747678
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388001A>C , CM000665.2:g.190388001A>C GRCh38
NC_000003.11:g.190105790A>C , CM000665.1:g.190105790A>C GRCh37
NC_000003.10:g.191588484A>C NCBI36
NG_008149.1:g.4950A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-119A>C ENSP00000264734.2:n.-119A>C
ENST00000468220.1:n.306+13398A>C
NM_006580.3:c.-119A>C NP_006571.1:n.-119A>C
NM_001378492.1:c.-93-236A>C NP_001365421.1:n.-93-236A>C
NM_001378493.1:c.-93-236A>C NP_001365422.1:n.-93-236A>C