Canonical Allele Identifier: CA89761517
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1031705285
MyVariant Identifiers: chr3:g.190120482G>A (hg19) chr3:g.190402693G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402693G>A , CM000665.2:g.190402693G>A GRCh38
NC_000003.11:g.190120482G>A , CM000665.1:g.190120482G>A GRCh37
NC_000003.10:g.191603176G>A NCBI36
NG_008149.1:g.19642G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.217+254G>A MANE Select ENSP00000264734.3:n.217+254G>A
ENST00000456423.2:c.115-7210G>A ENSP00000414136.2:n.115-7210G>A
ENST00000264734.2:c.427+254G>A ENSP00000264734.2:n.427+254G>A
ENST00000456423.1:c.325-7210G>A ENSP00000414136.1:n.325-7210G>A
ENST00000468220.1:n.409+254G>A
NM_006580.3:c.427+254G>A NP_006571.1:n.427+254G>A
NM_001378492.1:c.217+254G>A NP_001365421.1:n.217+254G>A
NM_001378493.1:c.217+254G>A NP_001365422.1:n.217+254G>A
NM_006580.4:c.217+254G>A MANE Select NP_006571.2:n.217+254G>A
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