Canonical Allele Identifier: CA89762818
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs944829588
gnomAD v3: 3-190404456-G-C
gnomAD v4: 3-190404456-G-C
MyVariant Identifiers: chr3:g.190404456G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404456G>C , CM000665.2:g.190404456G>C GRCh38
NC_000003.11:g.190122245G>C , CM000665.1:g.190122245G>C GRCh37
NC_000003.10:g.191604939G>C NCBI36
NG_008149.1:g.21405G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.218-306G>C MANE Select ENSP00000264734.3:n.218-306G>C
ENST00000456423.2:c.115-5447G>C ENSP00000414136.2:n.115-5447G>C
ENST00000264734.2:c.428-306G>C ENSP00000264734.2:n.428-306G>C
ENST00000456423.1:c.325-5447G>C ENSP00000414136.1:n.325-5447G>C
ENST00000468220.1:n.410-306G>C
NM_006580.3:c.428-306G>C NP_006571.1:n.428-306G>C
NM_001378492.1:c.218-306G>C NP_001365421.1:n.218-306G>C
NM_001378493.1:c.218-306G>C NP_001365422.1:n.218-306G>C
NM_006580.4:c.218-306G>C MANE Select NP_006571.2:n.218-306G>C
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