Canonical Allele Identifier: CA89749799

Gene: CLDN16

Linked Data

• dbSNP Id: rs960613047
• gnomAD v2: 3-190105948-T-C
• gnomAD v4: 3-190388159-T-C
• MyVariant Identifiers: chr3:g.190105948T>C (hg19) ; chr3:g.190388159T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388159T>C , CM000665.2:g.190388159T>C	GRCh38
NC_000003.11:g.190105948T>C , CM000665.1:g.190105948T>C	GRCh37
NC_000003.10:g.191588642T>C	NCBI36
NG_008149.1:g.5108T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-171T>C	ENSP00000414136.2:n.-171T>C
ENST00000264734.2:c.40T>C	ENSP00000264734.2:p.Tyr14His
ENST00000456423.1:c.40T>C	ENSP00000414136.1:p.Tyr14His
ENST00000468220.1:n.306+13556T>C
NM_006580.3:c.40T>C	NP_006571.1:p.Tyr14His
NM_001378492.1:c.-93-78T>C	NP_001365421.1:n.-93-78T>C
NM_001378493.1:c.-93-78T>C	NP_001365422.1:n.-93-78T>C