Canonical Allele Identifier: CA766253841

Gene: ATG16L1

Linked Data

• dbSNP Id: rs1472027300
• MyVariant Identifiers: chr2:g.233250049T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233250049T>C , CM000664.2:g.233250049T>C	GRCh38
NC_000002.11:g.234158695T>C , CM000664.1:g.234158695T>C	GRCh37
NC_000002.10:g.233823434T>C	NCBI36
NG_023038.1:g.3479T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000431917.5:c.-137-6053T>C	ENSP00000397512.1:n.-137-6053T>C