Canonical Allele Identifier: CA2759869846
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388023G>A , CM000665.2:g.190388023G>A GRCh38
NC_000003.11:g.190105812G>A , CM000665.1:g.190105812G>A GRCh37
NC_000003.10:g.191588506G>A NCBI36
NG_008149.1:g.4972G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-97G>A ENSP00000264734.2:n.-97G>A
ENST00000468220.1:n.306+13420G>A
NM_006580.3:c.-97G>A NP_006571.1:n.-97G>A
NM_001378492.1:c.-93-214G>A NP_001365421.1:n.-93-214G>A
NM_001378493.1:c.-93-214G>A NP_001365422.1:n.-93-214G>A