Canonical Allele Identifier: CA1043534202
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs1696252980

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250261G>A , CM000664.2:g.233250261G>A GRCh38
NC_000002.11:g.234158907G>A , CM000664.1:g.234158907G>A GRCh37
NC_000002.10:g.233823646G>A NCBI36
NG_023038.1:g.3691G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000431917.5:c.-137-5841G>A ENSP00000397512.1:n.-137-5841G>A