Canonical Allele Identifier: CA89763094

Gene: CLDN16

Linked Data

• dbSNP Id: rs966206029
• gnomAD v3: 3-190404691-T-G
• gnomAD v4: 3-190404691-T-G
• MyVariant Identifiers: chr3:g.190122480T>G (hg19) ; chr3:g.190404691T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404691T>G , CM000665.2:g.190404691T>G	GRCh38
NC_000003.11:g.190122480T>G , CM000665.1:g.190122480T>G	GRCh37
NC_000003.10:g.191605174T>G	NCBI36
NG_008149.1:g.21640T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.218-71T>G MANE Select	ENSP00000264734.3:n.218-71T>G
ENST00000456423.2:c.115-5212T>G	ENSP00000414136.2:n.115-5212T>G
ENST00000264734.2:c.428-71T>G	ENSP00000264734.2:n.428-71T>G
ENST00000456423.1:c.325-5212T>G	ENSP00000414136.1:n.325-5212T>G
ENST00000468220.1:n.410-71T>G
NM_006580.3:c.428-71T>G	NP_006571.1:n.428-71T>G
NM_001378492.1:c.218-71T>G	NP_001365421.1:n.218-71T>G
NM_001378493.1:c.218-71T>G	NP_001365422.1:n.218-71T>G
NM_006580.4:c.218-71T>G MANE Select	NP_006571.2:n.218-71T>G