Canonical Allele Identifier: CA766253878
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs1186070470
MyVariant Identifiers: chr2:g.233250123A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250123A>G , CM000664.2:g.233250123A>G GRCh38
NC_000002.11:g.234158769A>G , CM000664.1:g.234158769A>G GRCh37
NC_000002.10:g.233823508A>G NCBI36
NG_023038.1:g.3553A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000431917.5:c.-137-5979A>G ENSP00000397512.1:n.-137-5979A>G