Canonical Allele Identifier: CA2669054090
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs2108657920

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388026A>G , CM000665.2:g.190388026A>G GRCh38
NC_000003.11:g.190105815A>G , CM000665.1:g.190105815A>G GRCh37
NC_000003.10:g.191588509A>G NCBI36
NG_008149.1:g.4975A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-94A>G ENSP00000264734.2:n.-94A>G
ENST00000468220.1:n.306+13423A>G
NM_006580.3:c.-94A>G NP_006571.1:n.-94A>G
NM_001378492.1:c.-93-211A>G NP_001365421.1:n.-93-211A>G
NM_001378493.1:c.-93-211A>G NP_001365422.1:n.-93-211A>G