Canonical Allele Identifier: CA548497927
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1434152313
gnomAD v2: 3-190120411-T-C
gnomAD v3: 3-190402622-T-C
gnomAD v4: 3-190402622-T-C
MyVariant Identifiers: chr3:g.190120411T>C (hg19) chr3:g.190402622T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402622T>C , CM000665.2:g.190402622T>C GRCh38
NC_000003.11:g.190120411T>C , CM000665.1:g.190120411T>C GRCh37
NC_000003.10:g.191603105T>C NCBI36
NG_008149.1:g.19571T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.217+183T>C MANE Select ENSP00000264734.3:n.217+183T>C
ENST00000456423.2:c.115-7281T>C ENSP00000414136.2:n.115-7281T>C
ENST00000264734.2:c.427+183T>C ENSP00000264734.2:n.427+183T>C
ENST00000456423.1:c.325-7281T>C ENSP00000414136.1:n.325-7281T>C
ENST00000468220.1:n.409+183T>C
NM_006580.3:c.427+183T>C NP_006571.1:n.427+183T>C
NM_001378492.1:c.217+183T>C NP_001365421.1:n.217+183T>C
NM_001378493.1:c.217+183T>C NP_001365422.1:n.217+183T>C
NM_006580.4:c.217+183T>C MANE Select NP_006571.2:n.217+183T>C
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