Canonical Allele Identifier: CA1428759259
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1719047792
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404758C>G , CM000665.2:g.190404758C>G GRCh38
NC_000003.11:g.190122547C>G , CM000665.1:g.190122547C>G GRCh37
NC_000003.10:g.191605241C>G NCBI36
NG_008149.1:g.21707C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.218-4C>G MANE Select ENSP00000264734.3:n.218-4C>G
ENST00000456423.2:c.115-5145C>G ENSP00000414136.2:n.115-5145C>G
ENST00000264734.2:c.428-4C>G ENSP00000264734.2:n.428-4C>G
ENST00000456423.1:c.325-5145C>G ENSP00000414136.1:n.325-5145C>G
ENST00000468220.1:n.410-4C>G
NM_006580.3:c.428-4C>G NP_006571.1:n.428-4C>G
NM_001378492.1:c.218-4C>G NP_001365421.1:n.218-4C>G
NM_001378493.1:c.218-4C>G NP_001365422.1:n.218-4C>G
NM_006580.4:c.218-4C>G MANE Select NP_006571.2:n.218-4C>G
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