Canonical Allele Identifier: CA042828

Gene:

Linked Data

• ClinVar Variation Id: 29906
• ClinVar RCV Id: RCV000022790
• dbSNP Id: rs180195
• gnomAD v2: 8-133877623-A-G
• gnomAD v3: 8-132865378-A-G
• gnomAD v4: 8-132865378-A-G
• MyVariant Identifiers: chr8:g.133877623A>G (hg19) ; chr8:g.132865378A>G (hg38)
• PubMed: PMID:21757724

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132865378A>G , CM000670.2:g.132865378A>G	GRCh38
NC_000008.10:g.133877623A>G , CM000670.1:g.133877623A>G	GRCh37
NC_000008.9:g.133946805A>G	NCBI36
NG_015832.1:g.3419A>G