Canonical Allele Identifier: CA2753795
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 1209150
ClinVar RCV Id: RCV001577721
dbSNP Id: rs77798557
ExAC: 3:190120252 G / T
gnomAD v2: 3-190120252-G-T
gnomAD v3: 3-190402463-G-T
gnomAD v4: 3-190402463-G-T
MyVariant Identifiers: chr3:g.190120252G>T (hg19) chr3:g.190402463G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402463G>T , CM000665.2:g.190402463G>T GRCh38
NC_000003.11:g.190120252G>T , CM000665.1:g.190120252G>T GRCh37
NC_000003.10:g.191602946G>T NCBI36
NG_008149.1:g.19412G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.217+24G>T MANE Select ENSP00000264734.3:n.217+24G>T
ENST00000456423.2:c.115-7440G>T ENSP00000414136.2:n.115-7440G>T
ENST00000264734.2:c.427+24G>T ENSP00000264734.2:n.427+24G>T
ENST00000456423.1:c.325-7440G>T ENSP00000414136.1:n.325-7440G>T
ENST00000468220.1:n.409+24G>T
NM_006580.3:c.427+24G>T NP_006571.1:n.427+24G>T
NM_001378492.1:c.217+24G>T NP_001365421.1:n.217+24G>T
NM_001378493.1:c.217+24G>T NP_001365422.1:n.217+24G>T
NM_006580.4:c.217+24G>T MANE Select NP_006571.2:n.217+24G>T
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