Canonical Allele Identifier: CA437637149
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190106010A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388221A>G , CM000665.2:g.190388221A>G GRCh38
NC_000003.11:g.190106010A>G , CM000665.1:g.190106010A>G GRCh37
NC_000003.10:g.191588704A>G NCBI36
NG_008149.1:g.5170A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.-109A>G MANE Select ENSP00000264734.3:n.-109A>G
ENST00000456423.2:c.-109A>G ENSP00000414136.2:n.-109A>G
ENST00000264734.2:c.102A>G ENSP00000264734.2:p.Val34=
ENST00000456423.1:c.102A>G ENSP00000414136.1:p.Val34=
ENST00000468220.1:n.306+13618A>G
NM_006580.3:c.102A>G NP_006571.1:p.Val34=
NM_001378492.1:c.-93-16A>G NP_001365421.1:n.-93-16A>G
NM_001378493.1:c.-93-16A>G NP_001365422.1:n.-93-16A>G
NM_006580.4:c.-109A>G MANE Select NP_006571.2:n.-109A>G
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