Canonical Allele Identifier: CA67532924
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs967397432
gnomAD v2: 2-234158955-A-G
gnomAD v3: 2-233250309-A-G
gnomAD v4: 2-233250309-A-G
MyVariant Identifiers: chr2:g.234158955A>G (hg19) chr2:g.233250309A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250309A>G , CM000664.2:g.233250309A>G GRCh38
NC_000002.11:g.234158955A>G , CM000664.1:g.234158955A>G GRCh37
NC_000002.10:g.233823694A>G NCBI36
NG_023038.1:g.3739A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000431917.5:c.-137-5793A>G ENSP00000397512.1:n.-137-5793A>G
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