Canonical Allele Identifier: CA766253911
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs1266494319
MyVariant Identifiers: chr2:g.233250285C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250285C>T , CM000664.2:g.233250285C>T GRCh38
NC_000002.11:g.234158931C>T , CM000664.1:g.234158931C>T GRCh37
NC_000002.10:g.233823670C>T NCBI36
NG_023038.1:g.3715C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000431917.5:c.-137-5817C>T ENSP00000397512.1:n.-137-5817C>T
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