Canonical Allele Identifier: CA548494038
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1413743935
gnomAD v2: 3-190105808-T-G
gnomAD v3: 3-190388019-T-G
gnomAD v4: 3-190388019-T-G
MyVariant Identifiers: chr3:g.190105808T>G (hg19) chr3:g.190388019T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388019T>G , CM000665.2:g.190388019T>G GRCh38
NC_000003.11:g.190105808T>G , CM000665.1:g.190105808T>G GRCh37
NC_000003.10:g.191588502T>G NCBI36
NG_008149.1:g.4968T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-101T>G ENSP00000264734.2:n.-101T>G
ENST00000468220.1:n.306+13416T>G
NM_006580.3:c.-101T>G NP_006571.1:n.-101T>G
NM_001378492.1:c.-93-218T>G NP_001365421.1:n.-93-218T>G
NM_001378493.1:c.-93-218T>G NP_001365422.1:n.-93-218T>G
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