Canonical Allele Identifier: CA89761309
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs768289133
gnomAD v4: 3-190402500-A-C
MyVariant Identifiers: chr3:g.190120289A>C (hg19) chr3:g.190402500A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402500A>C , CM000665.2:g.190402500A>C GRCh38
NC_000003.11:g.190120289A>C , CM000665.1:g.190120289A>C GRCh37
NC_000003.10:g.191602983A>C NCBI36
NG_008149.1:g.19449A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.217+61A>C MANE Select ENSP00000264734.3:n.217+61A>C
ENST00000456423.2:c.115-7403A>C ENSP00000414136.2:n.115-7403A>C
ENST00000264734.2:c.427+61A>C ENSP00000264734.2:n.427+61A>C
ENST00000456423.1:c.325-7403A>C ENSP00000414136.1:n.325-7403A>C
ENST00000468220.1:n.409+61A>C
NM_006580.3:c.427+61A>C NP_006571.1:n.427+61A>C
NM_001378492.1:c.217+61A>C NP_001365421.1:n.217+61A>C
NM_001378493.1:c.217+61A>C NP_001365422.1:n.217+61A>C
NM_006580.4:c.217+61A>C MANE Select NP_006571.2:n.217+61A>C
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