Canonical Allele Identifier: CA89766153
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs958223859

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408178C>T , CM000665.2:g.190408178C>T GRCh38
NC_000003.11:g.190125967C>T , CM000665.1:g.190125967C>T GRCh37
NC_000003.10:g.191608661C>T NCBI36
NG_008149.1:g.25127C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.383-136C>T MANE Select ENSP00000264734.3:n.383-136C>T
ENST00000456423.2:c.115-1725C>T ENSP00000414136.2:n.115-1725C>T
ENST00000264734.2:c.593-136C>T ENSP00000264734.2:n.593-136C>T
ENST00000456423.1:c.325-1725C>T ENSP00000414136.1:n.325-1725C>T
NM_006580.3:c.593-136C>T NP_006571.1:n.593-136C>T
NM_001378492.1:c.383-136C>T NP_001365421.1:n.383-136C>T
NM_001378493.1:c.383-136C>T NP_001365422.1:n.383-136C>T
NM_006580.4:c.383-136C>T MANE Select NP_006571.2:n.383-136C>T