Canonical Allele Identifier: CA2577990708
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388046T>G , CM000665.2:g.190388046T>G GRCh38
NC_000003.11:g.190105835T>G , CM000665.1:g.190105835T>G GRCh37
NC_000003.10:g.191588529T>G NCBI36
NG_008149.1:g.4995T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-74T>G ENSP00000264734.2:n.-74T>G
ENST00000468220.1:n.306+13443T>G
NM_006580.3:c.-74T>G NP_006571.1:n.-74T>G
NM_001378492.1:c.-93-191T>G NP_001365421.1:n.-93-191T>G
NM_001378493.1:c.-93-191T>G NP_001365422.1:n.-93-191T>G