Canonical Allele Identifier: CA2753678
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs758074559

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388132A>G , CM000665.2:g.190388132A>G GRCh38
NC_000003.11:g.190105921A>G , CM000665.1:g.190105921A>G GRCh37
NC_000003.10:g.191588615A>G NCBI36
NG_008149.1:g.5081A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000456423.2:c.-198A>G ENSP00000414136.2:n.-198A>G
ENST00000264734.2:c.13A>G ENSP00000264734.2:p.Thr5Ala
ENST00000456423.1:c.13A>G ENSP00000414136.1:p.Thr5Ala
ENST00000468220.1:n.306+13529A>G
NM_006580.3:c.13A>G NP_006571.1:p.Thr5Ala
NM_001378492.1:c.-93-105A>G NP_001365421.1:n.-93-105A>G
NM_001378493.1:c.-93-105A>G NP_001365422.1:n.-93-105A>G