Canonical Allele Identifier: CA67532735
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs946038865
MyVariant Identifiers: chr2:g.233250012A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250012A>T , CM000664.2:g.233250012A>T GRCh38
NC_000002.11:g.234158658A>T , CM000664.1:g.234158658A>T GRCh37
NC_000002.10:g.233823397A>T NCBI36
NG_023038.1:g.3442A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000431917.5:c.-137-6090A>T ENSP00000397512.1:n.-137-6090A>T