Canonical Allele Identifier: CA1057683999

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718546445
• gnomAD v3: 3-190387943-A-G
• gnomAD v4: 3-190387943-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190387943A>G , CM000665.2:g.190387943A>G	GRCh38
NC_000003.11:g.190105732A>G , CM000665.1:g.190105732A>G	GRCh37
NC_000003.10:g.191588426A>G	NCBI36
NG_008149.1:g.4892A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-177A>G	ENSP00000264734.2:n.-177A>G
ENST00000468220.1:n.306+13340A>G
NM_006580.3:c.-177A>G	NP_006571.1:n.-177A>G
NM_001378492.1:c.-93-294A>G	NP_001365421.1:n.-93-294A>G
NM_001378493.1:c.-93-294A>G	NP_001365422.1:n.-93-294A>G