Canonical Allele Identifier: CA1335653514
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs1696254054

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250284A>C , CM000664.2:g.233250284A>C GRCh38
NC_000002.11:g.234158930A>C , CM000664.1:g.234158930A>C GRCh37
NC_000002.10:g.233823669A>C NCBI36
NG_023038.1:g.3714A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000431917.5:c.-137-5818A>C ENSP00000397512.1:n.-137-5818A>C