Canonical Allele Identifier: CA766253913

Gene: ATG16L1

Linked Data

• dbSNP Id: rs1341153186
• MyVariant Identifiers: chr2:g.233250290G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233250290G>A , CM000664.2:g.233250290G>A	GRCh38
NC_000002.11:g.234158936G>A , CM000664.1:g.234158936G>A	GRCh37
NC_000002.10:g.233823675G>A	NCBI36
NG_023038.1:g.3720G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431917.5:c.-137-5812G>A	ENSP00000397512.1:n.-137-5812G>A