Canonical Allele Identifier: CA437637264
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs2108658210
MyVariant Identifiers: chr3:g.190106100T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388311T>G , CM000665.2:g.190388311T>G GRCh38
NC_000003.11:g.190106100T>G , CM000665.1:g.190106100T>G GRCh37
NC_000003.10:g.191588794T>G NCBI36
NG_008149.1:g.5260T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.-19T>G MANE Select ENSP00000264734.3:n.-19T>G
ENST00000456423.2:c.-19T>G ENSP00000414136.2:n.-19T>G
ENST00000264734.2:c.192T>G ENSP00000264734.2:p.Pro64=
ENST00000456423.1:c.192T>G ENSP00000414136.1:p.Pro64=
ENST00000468220.1:n.306+13708T>G
NM_006580.3:c.192T>G NP_006571.1:p.Pro64=
NM_001378492.1:c.-19T>G NP_001365421.1:n.-19T>G
NM_001378493.1:c.-19T>G NP_001365422.1:n.-19T>G
NM_006580.4:c.-19T>G MANE Select NP_006571.2:n.-19T>G
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