Canonical Allele Identifier: CA2669054136

Gene: CLDN16

Linked Data

• dbSNP Id: rs2108657971
• gnomAD v4: 3-190388105-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388105T>C , CM000665.2:g.190388105T>C	GRCh38
NC_000003.11:g.190105894T>C , CM000665.1:g.190105894T>C	GRCh37
NC_000003.10:g.191588588T>C	NCBI36
NG_008149.1:g.5054T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-15T>C	ENSP00000264734.2:n.-15T>C
ENST00000468220.1:n.306+13502T>C
NM_006580.3:c.-15T>C	NP_006571.1:n.-15T>C
NM_001378492.1:c.-93-132T>C	NP_001365421.1:n.-93-132T>C
NM_001378493.1:c.-93-132T>C	NP_001365422.1:n.-93-132T>C