Canonical Allele Identifier: CA1335653947
Gene: ATG16L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233251240A= , CM000664.2:g.233251240A= GRCh38
NC_000002.11:g.234159886A= , CM000664.1:g.234159886A= GRCh37
NC_000002.10:g.233824625A= NCBI36
NG_023038.1:g.4670A=

Transcript Alleles

HGVS Amino-acid change
ENST00000431917.5:c.-137-4862A= ENSP00000397512.1:n.-137-4862A=