Canonical Allele Identifier: CA67532768
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs866449843
MyVariant Identifiers: chr2:g.234158709G>A (hg19) chr2:g.233250063G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250063G>A , CM000664.2:g.233250063G>A GRCh38
NC_000002.11:g.234158709G>A , CM000664.1:g.234158709G>A GRCh37
NC_000002.10:g.233823448G>A NCBI36
NG_023038.1:g.3493G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000431917.5:c.-137-6039G>A ENSP00000397512.1:n.-137-6039G>A
Search 100 bp 5'
Search 100 bp 3'