Canonical Allele Identifier: CA89749527
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1015248875
MyVariant Identifiers: chr3:g.190387970C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387970C>G , CM000665.2:g.190387970C>G GRCh38
NC_000003.11:g.190105759C>G , CM000665.1:g.190105759C>G GRCh37
NC_000003.10:g.191588453C>G NCBI36
NG_008149.1:g.4919C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-150C>G ENSP00000264734.2:n.-150C>G
ENST00000468220.1:n.306+13367C>G
NM_006580.3:c.-150C>G NP_006571.1:n.-150C>G
NM_001378492.1:c.-93-267C>G NP_001365421.1:n.-93-267C>G
NM_001378493.1:c.-93-267C>G NP_001365422.1:n.-93-267C>G