Canonical Allele Identifier: CA2669054080
Gene: CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190388012-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388012C>A , CM000665.2:g.190388012C>A GRCh38
NC_000003.11:g.190105801C>A , CM000665.1:g.190105801C>A GRCh37
NC_000003.10:g.191588495C>A NCBI36
NG_008149.1:g.4961C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-108C>A ENSP00000264734.2:n.-108C>A
ENST00000468220.1:n.306+13409C>A
NM_006580.3:c.-108C>A NP_006571.1:n.-108C>A
NM_001378492.1:c.-93-225C>A NP_001365421.1:n.-93-225C>A
NM_001378493.1:c.-93-225C>A NP_001365422.1:n.-93-225C>A
Search 100 bp 5'
Search 100 bp 3'