Canonical Allele Identifier: CA67532911

Gene: ATG16L1

Linked Data

• dbSNP Id: rs1046770632
• MyVariant Identifiers: chr2:g.234158877C>T (hg19) ; chr2:g.233250231C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233250231C>T , CM000664.2:g.233250231C>T	GRCh38
NC_000002.11:g.234158877C>T , CM000664.1:g.234158877C>T	GRCh37
NC_000002.10:g.233823616C>T	NCBI36
NG_023038.1:g.3661C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000431917.5:c.-137-5871C>T	ENSP00000397512.1:n.-137-5871C>T