Canonical Allele Identifier: CA1335653489
Gene: ATG16L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250211C= , CM000664.2:g.233250211C= GRCh38
NC_000002.11:g.234158857C= , CM000664.1:g.234158857C= GRCh37
NC_000002.10:g.233823596C= NCBI36
NG_023038.1:g.3641C=

Transcript Alleles

HGVS Amino-acid change
ENST00000431917.5:c.-137-5891C= ENSP00000397512.1:n.-137-5891C=