Canonical Allele Identifier: CA437418361
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190120167A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402378A>C , CM000665.2:g.190402378A>C GRCh38
NC_000003.11:g.190120167A>C , CM000665.1:g.190120167A>C GRCh37
NC_000003.10:g.191602861A>C NCBI36
NG_008149.1:g.19327A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.156A>C MANE Select ENSP00000264734.3:p.Thr52=
ENST00000456423.2:c.115-7525A>C ENSP00000414136.2:n.115-7525A>C
ENST00000264734.2:c.366A>C ENSP00000264734.2:p.Thr122=
ENST00000456423.1:c.325-7525A>C ENSP00000414136.1:n.325-7525A>C
ENST00000468220.1:n.348A>C
NM_006580.3:c.366A>C NP_006571.1:p.Thr122=
NM_001378492.1:c.156A>C NP_001365421.1:p.Thr52=
NM_001378493.1:c.156A>C NP_001365422.1:p.Thr52=
NM_006580.4:c.156A>C MANE Select NP_006571.2:p.Thr52=
Search 100 bp 5'
Search 100 bp 3'