Canonical Allele Identifier: CA67532958
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs939248641
MyVariant Identifiers: chr2:g.233250330C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250330C>G , CM000664.2:g.233250330C>G GRCh38
NC_000002.11:g.234158976C>G , CM000664.1:g.234158976C>G GRCh37
NC_000002.10:g.233823715C>G NCBI36
NG_023038.1:g.3760C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000431917.5:c.-137-5772C>G ENSP00000397512.1:n.-137-5772C>G