Canonical Allele Identifier: CA10576176

Gene:

Linked Data

• dbSNP Id: rs7196161
• gnomAD v2: 16-31110981-G-A
• gnomAD v3: 16-31099660-G-A
• gnomAD v4: 16-31099660-G-A
• MyVariant Identifiers: chr16:g.31110981G>A (hg19) ; chr16:g.31099660G>A (hg38)
• PubMed: PMID:21383771 ; PMID:22992668 ; PMID:24019055

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31099660G>A , CM000678.2:g.31099660G>A	GRCh38
NC_000016.9:g.31110981G>A , CM000678.1:g.31110981G>A	GRCh37
NC_000016.8:g.31018482G>A	NCBI36
NG_011564.1:g.296C>T