Canonical Allele Identifier: CA648077153
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388116G>T , CM000665.2:g.190388116G>T GRCh38
NC_000003.11:g.190105905G>T , CM000665.1:g.190105905G>T GRCh37
NC_000003.10:g.191588599G>T NCBI36
NG_008149.1:g.5065G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-4G>T ENSP00000264734.2:n.-4G>T
ENST00000468220.1:n.306+13513G>T
NM_006580.3:c.-4G>T NP_006571.1:n.-4G>T
NM_001378492.1:c.-93-121G>T NP_001365421.1:n.-93-121G>T
NM_001378493.1:c.-93-121G>T NP_001365422.1:n.-93-121G>T