Canonical Allele Identifier: CA89745654
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs16865344

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190322595C>G , CM000665.2:g.190322595C>G GRCh38
NC_000003.11:g.190040384C>G , CM000665.1:g.190040384C>G GRCh37
NC_000003.10:g.191523078C>G NCBI36
NG_021418.1:g.4852G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000468220.1:n.55C>G
NM_001378492.1:c.-279+7536C>G NP_001365421.1:n.-279+7536C>G
NM_001378493.1:c.-279+32004C>G NP_001365422.1:n.-279+32004C>G