Canonical Allele Identifier: CA766253897

Gene: ATG16L1

Linked Data

• dbSNP Id: rs10210302
• gnomAD v3: 2-233250193-C-A
• gnomAD v4: 2-233250193-C-A
• MyVariant Identifiers: chr2:g.234158839C>A (hg19) ; chr2:g.233250193C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233250193C>A , CM000664.2:g.233250193C>A	GRCh38
NC_000002.11:g.234158839C>A , CM000664.1:g.234158839C>A	GRCh37
NC_000002.10:g.233823578C>A	NCBI36
NG_023038.1:g.3623C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000431917.5:c.-137-5909C>A	ENSP00000397512.1:n.-137-5909C>A