Canonical Allele Identifier: CA67532755
Gene: ATG16L1 HGNC NCBI

Linked Data

dbSNP Id: rs1019147796
MyVariant Identifiers: chr2:g.234158672T>C (hg19) chr2:g.233250026T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233250026T>C , CM000664.2:g.233250026T>C GRCh38
NC_000002.11:g.234158672T>C , CM000664.1:g.234158672T>C GRCh37
NC_000002.10:g.233823411T>C NCBI36
NG_023038.1:g.3456T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000431917.5:c.-137-6076T>C ENSP00000397512.1:n.-137-6076T>C
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