Canonical Allele Identifier: CA437637038

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190388128-C-T
• MyVariant Identifiers: chr3:g.190105917C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388128C>T , CM000665.2:g.190388128C>T	GRCh38
NC_000003.11:g.190105917C>T , CM000665.1:g.190105917C>T	GRCh37
NC_000003.10:g.191588611C>T	NCBI36
NG_008149.1:g.5077C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-202C>T	ENSP00000414136.2:n.-202C>T
ENST00000264734.2:c.9C>T	ENSP00000264734.2:p.Ser3=
ENST00000456423.1:c.9C>T	ENSP00000414136.1:p.Ser3=
ENST00000468220.1:n.306+13525C>T
NM_006580.3:c.9C>T	NP_006571.1:p.Ser3=
NM_001378492.1:c.-93-109C>T	NP_001365421.1:n.-93-109C>T
NM_001378493.1:c.-93-109C>T	NP_001365422.1:n.-93-109C>T