Canonical Allele Identifier: CA184586763

Gene:

Linked Data

• dbSNP Id: rs10088262
• gnomAD v2: 8-124765702-A-G
• gnomAD v3: 8-123753462-A-G
• gnomAD v4: 8-123753462-A-G
• MyVariant Identifiers: chr8:g.124765702A>G (hg19) ; chr8:g.123753462A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123753462A>G , CM000670.2:g.123753462A>G	GRCh38
NC_000008.10:g.124765702A>G , CM000670.1:g.124765702A>G	GRCh37
NC_000008.9:g.124834883A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_928607.1:n.153-11321A>G
XR_928607.3:n.324-11321A>G