Canonical Allele Identifier: CA548494040
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1165566495
gnomAD v2: 3-190105843-C-A
gnomAD v3: 3-190388054-C-A
gnomAD v4: 3-190388054-C-A
MyVariant Identifiers: chr3:g.190105843C>A (hg19) chr3:g.190388054C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388054C>A , CM000665.2:g.190388054C>A GRCh38
NC_000003.11:g.190105843C>A , CM000665.1:g.190105843C>A GRCh37
NC_000003.10:g.191588537C>A NCBI36
NG_008149.1:g.5003C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-66C>A ENSP00000264734.2:n.-66C>A
ENST00000468220.1:n.306+13451C>A
NM_006580.3:c.-66C>A NP_006571.1:n.-66C>A
NM_001378492.1:c.-93-183C>A NP_001365421.1:n.-93-183C>A
NM_001378493.1:c.-93-183C>A NP_001365422.1:n.-93-183C>A
Search 100 bp 5'
Search 100 bp 3'