Canonical Allele Identifier: CA89749541
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs187663828
gnomAD v2: 3-190105763-G-A
gnomAD v3: 3-190387974-G-A
gnomAD v4: 3-190387974-G-A
MyVariant Identifiers: chr3:g.190105763G>A (hg19) chr3:g.190387974G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387974G>A , CM000665.2:g.190387974G>A GRCh38
NC_000003.11:g.190105763G>A , CM000665.1:g.190105763G>A GRCh37
NC_000003.10:g.191588457G>A NCBI36
NG_008149.1:g.4923G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-146G>A ENSP00000264734.2:n.-146G>A
ENST00000468220.1:n.306+13371G>A
NM_006580.3:c.-146G>A NP_006571.1:n.-146G>A
NM_001378492.1:c.-93-263G>A NP_001365421.1:n.-93-263G>A
NM_001378493.1:c.-93-263G>A NP_001365422.1:n.-93-263G>A
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