Canonical Allele Identifier: CA2701677195
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs1696255469

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250302G>A , CM000664.2:g.233250302G>A GRCh38
NC_000002.11:g.234158948G>A , CM000664.1:g.234158948G>A GRCh37
NC_000002.10:g.233823687G>A NCBI36
NG_023038.1:g.3732G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000431917.5:c.-137-5800G>A ENSP00000397512.1:n.-137-5800G>A