Canonical Allele Identifier: CA355762109

Gene: CLDN16

Linked Data

• dbSNP Id: rs1322689733
• MyVariant Identifiers: chr3:g.190105913C>G (hg19) ; chr3:g.190388124C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388124C>G , CM000665.2:g.190388124C>G	GRCh38
NC_000003.11:g.190105913C>G , CM000665.1:g.190105913C>G	GRCh37
NC_000003.10:g.191588607C>G	NCBI36
NG_008149.1:g.5073C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-206C>G	ENSP00000414136.2:n.-206C>G
ENST00000264734.2:c.5C>G	ENSP00000264734.2:p.Thr2Ser
ENST00000456423.1:c.5C>G	ENSP00000414136.1:p.Thr2Ser
ENST00000468220.1:n.306+13521C>G
NM_006580.3:c.5C>G	NP_006571.1:p.Thr2Ser
NM_001378492.1:c.-93-113C>G	NP_001365421.1:n.-93-113C>G
NM_001378493.1:c.-93-113C>G	NP_001365422.1:n.-93-113C>G