Canonical Allele Identifier: CA1043534193
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs1696250650

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250220C>T , CM000664.2:g.233250220C>T GRCh38
NC_000002.11:g.234158866C>T , CM000664.1:g.234158866C>T GRCh37
NC_000002.10:g.233823605C>T NCBI36
NG_023038.1:g.3650C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000431917.5:c.-137-5882C>T ENSP00000397512.1:n.-137-5882C>T