Canonical Allele Identifier: CA89761512
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs189008859
gnomAD v2: 3-190120474-C-A
gnomAD v3: 3-190402685-C-A
gnomAD v4: 3-190402685-C-A
MyVariant Identifiers: chr3:g.190120474C>A (hg19) chr3:g.190402685C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402685C>A , CM000665.2:g.190402685C>A GRCh38
NC_000003.11:g.190120474C>A , CM000665.1:g.190120474C>A GRCh37
NC_000003.10:g.191603168C>A NCBI36
NG_008149.1:g.19634C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.217+246C>A MANE Select ENSP00000264734.3:n.217+246C>A
ENST00000456423.2:c.115-7218C>A ENSP00000414136.2:n.115-7218C>A
ENST00000264734.2:c.427+246C>A ENSP00000264734.2:n.427+246C>A
ENST00000456423.1:c.325-7218C>A ENSP00000414136.1:n.325-7218C>A
ENST00000468220.1:n.409+246C>A
NM_006580.3:c.427+246C>A NP_006571.1:n.427+246C>A
NM_001378492.1:c.217+246C>A NP_001365421.1:n.217+246C>A
NM_001378493.1:c.217+246C>A NP_001365422.1:n.217+246C>A
NM_006580.4:c.217+246C>A MANE Select NP_006571.2:n.217+246C>A
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