Canonical Allele Identifier: CA355766290
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 802037
ClinVar RCV Id: RCV000987375
dbSNP Id: rs1577430815
MyVariant Identifiers: chr3:g.190122715G>C (hg19) chr3:g.190404926G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404926G>C , CM000665.2:g.190404926G>C GRCh38
NC_000003.11:g.190122715G>C , CM000665.1:g.190122715G>C GRCh37
NC_000003.10:g.191605409G>C NCBI36
NG_008149.1:g.21875G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.382G>C MANE Select ENSP00000264734.3:p.Gly128Arg
ENST00000456423.2:c.115-4977G>C ENSP00000414136.2:n.115-4977G>C
ENST00000264734.2:c.592G>C ENSP00000264734.2:p.Gly198Arg
ENST00000456423.1:c.325-4977G>C ENSP00000414136.1:n.325-4977G>C
ENST00000468220.1:n.574G>C
NM_006580.3:c.592G>C NP_006571.1:p.Gly198Arg
NM_001378492.1:c.382G>C NP_001365421.1:p.Gly128Arg
NM_001378493.1:c.382G>C NP_001365422.1:p.Gly128Arg
NM_006580.4:c.382G>C MANE Select NP_006571.2:p.Gly128Arg
Search 100 bp 5'
Search 100 bp 3'