Canonical Allele Identifier: CA1428775451
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1413743935
gnomAD v4: 3-190388019-T-C
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-101T>C ENSP00000264734.2:n.-101T>C
ENST00000468220.1:n.306+13416T>C
NM_006580.3:c.-101T>C NP_006571.1:n.-101T>C
NM_001378492.1:c.-93-218T>C NP_001365421.1:n.-93-218T>C
NM_001378493.1:c.-93-218T>C NP_001365422.1:n.-93-218T>C
Search 100 bp 5'
Search 100 bp 3'