Canonical Allele Identifier: CA2759869848
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388053C>T , CM000665.2:g.190388053C>T GRCh38
NC_000003.11:g.190105842C>T , CM000665.1:g.190105842C>T GRCh37
NC_000003.10:g.191588536C>T NCBI36
NG_008149.1:g.5002C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-67C>T ENSP00000264734.2:n.-67C>T
ENST00000468220.1:n.306+13450C>T
NM_006580.3:c.-67C>T NP_006571.1:n.-67C>T
NM_001378492.1:c.-93-184C>T NP_001365421.1:n.-93-184C>T
NM_001378493.1:c.-93-184C>T NP_001365422.1:n.-93-184C>T