Canonical Allele Identifier: CA89762888

Gene: CLDN16

Linked Data

• dbSNP Id: rs914781079
• MyVariant Identifiers: chr3:g.190122291C>T (hg19) ; chr3:g.190404502C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404502C>T , CM000665.2:g.190404502C>T	GRCh38
NC_000003.11:g.190122291C>T , CM000665.1:g.190122291C>T	GRCh37
NC_000003.10:g.191604985C>T	NCBI36
NG_008149.1:g.21451C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-260C>T MANE Select	ENSP00000264734.3:n.218-260C>T
ENST00000456423.2:c.115-5401C>T	ENSP00000414136.2:n.115-5401C>T
ENST00000264734.2:c.428-260C>T	ENSP00000264734.2:n.428-260C>T
ENST00000456423.1:c.325-5401C>T	ENSP00000414136.1:n.325-5401C>T
ENST00000468220.1:n.410-260C>T
NM_006580.3:c.428-260C>T	NP_006571.1:n.428-260C>T
NM_001378492.1:c.218-260C>T	NP_001365421.1:n.218-260C>T
NM_001378493.1:c.218-260C>T	NP_001365422.1:n.218-260C>T
NM_006580.4:c.218-260C>T MANE Select	NP_006571.2:n.218-260C>T