Canonical Allele Identifier: CA904290944
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs146256555
MyVariant Identifiers: chr3:g.190125864G>C (hg19) chr3:g.190408075G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408075G>C , CM000665.2:g.190408075G>C GRCh38
NC_000003.11:g.190125864G>C , CM000665.1:g.190125864G>C GRCh37
NC_000003.10:g.191608558G>C NCBI36
NG_008149.1:g.25024G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.383-239G>C MANE Select ENSP00000264734.3:n.383-239G>C
ENST00000456423.2:c.115-1828G>C ENSP00000414136.2:n.115-1828G>C
ENST00000264734.2:c.593-239G>C ENSP00000264734.2:n.593-239G>C
ENST00000456423.1:c.325-1828G>C ENSP00000414136.1:n.325-1828G>C
NM_006580.3:c.593-239G>C NP_006571.1:n.593-239G>C
NM_001378492.1:c.383-239G>C NP_001365421.1:n.383-239G>C
NM_001378493.1:c.383-239G>C NP_001365422.1:n.383-239G>C
NM_006580.4:c.383-239G>C MANE Select NP_006571.2:n.383-239G>C
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