Canonical Allele Identifier: CA89766174
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs955133367
gnomAD v4: 3-190408193-T-A
MyVariant Identifiers: chr3:g.190125982T>A (hg19) chr3:g.190408193T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408193T>A , CM000665.2:g.190408193T>A GRCh38
NC_000003.11:g.190125982T>A , CM000665.1:g.190125982T>A GRCh37
NC_000003.10:g.191608676T>A NCBI36
NG_008149.1:g.25142T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.383-121T>A MANE Select ENSP00000264734.3:n.383-121T>A
ENST00000456423.2:c.115-1710T>A ENSP00000414136.2:n.115-1710T>A
ENST00000264734.2:c.593-121T>A ENSP00000264734.2:n.593-121T>A
ENST00000456423.1:c.325-1710T>A ENSP00000414136.1:n.325-1710T>A
NM_006580.3:c.593-121T>A NP_006571.1:n.593-121T>A
NM_001378492.1:c.383-121T>A NP_001365421.1:n.383-121T>A
NM_001378493.1:c.383-121T>A NP_001365422.1:n.383-121T>A
NM_006580.4:c.383-121T>A MANE Select NP_006571.2:n.383-121T>A
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