Canonical Allele Identifier: CA437637172
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190106028A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388239A>C , CM000665.2:g.190388239A>C GRCh38
NC_000003.11:g.190106028A>C , CM000665.1:g.190106028A>C GRCh37
NC_000003.10:g.191588722A>C NCBI36
NG_008149.1:g.5188A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.-91A>C MANE Select ENSP00000264734.3:n.-91A>C
ENST00000456423.2:c.-91A>C ENSP00000414136.2:n.-91A>C
ENST00000264734.2:c.120A>C ENSP00000264734.2:p.Val40=
ENST00000456423.1:c.120A>C ENSP00000414136.1:p.Val40=
ENST00000468220.1:n.306+13636A>C
NM_006580.3:c.120A>C NP_006571.1:p.Val40=
NM_001378492.1:c.-91A>C NP_001365421.1:n.-91A>C
NM_001378493.1:c.-91A>C NP_001365422.1:n.-91A>C
NM_006580.4:c.-91A>C MANE Select NP_006571.2:n.-91A>C
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