Canonical Allele Identifier: CA1057684009
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1718547332

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387971C>T , CM000665.2:g.190387971C>T GRCh38
NC_000003.11:g.190105760C>T , CM000665.1:g.190105760C>T GRCh37
NC_000003.10:g.191588454C>T NCBI36
NG_008149.1:g.4920C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-149C>T ENSP00000264734.2:n.-149C>T
ENST00000468220.1:n.306+13368C>T
NM_006580.3:c.-149C>T NP_006571.1:n.-149C>T
NM_001378492.1:c.-93-266C>T NP_001365421.1:n.-93-266C>T
NM_001378493.1:c.-93-266C>T NP_001365422.1:n.-93-266C>T