Canonical Allele Identifier: CA89766178
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs941466784

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408222C>T , CM000665.2:g.190408222C>T GRCh38
NC_000003.11:g.190126011C>T , CM000665.1:g.190126011C>T GRCh37
NC_000003.10:g.191608705C>T NCBI36
NG_008149.1:g.25171C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.383-92C>T MANE Select ENSP00000264734.3:n.383-92C>T
ENST00000456423.2:c.115-1681C>T ENSP00000414136.2:n.115-1681C>T
ENST00000264734.2:c.593-92C>T ENSP00000264734.2:n.593-92C>T
ENST00000456423.1:c.325-1681C>T ENSP00000414136.1:n.325-1681C>T
NM_006580.3:c.593-92C>T NP_006571.1:n.593-92C>T
NM_001378492.1:c.383-92C>T NP_001365421.1:n.383-92C>T
NM_001378493.1:c.383-92C>T NP_001365422.1:n.383-92C>T
NM_006580.4:c.383-92C>T MANE Select NP_006571.2:n.383-92C>T