Canonical Allele Identifier: CA2669054062
Gene: CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190387993-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387993G>T , CM000665.2:g.190387993G>T GRCh38
NC_000003.11:g.190105782G>T , CM000665.1:g.190105782G>T GRCh37
NC_000003.10:g.191588476G>T NCBI36
NG_008149.1:g.4942G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-127G>T ENSP00000264734.2:n.-127G>T
ENST00000468220.1:n.306+13390G>T
NM_006580.3:c.-127G>T NP_006571.1:n.-127G>T
NM_001378492.1:c.-93-244G>T NP_001365421.1:n.-93-244G>T
NM_001378493.1:c.-93-244G>T NP_001365422.1:n.-93-244G>T
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