Canonical Allele Identifier: CA77246651

Gene:

Linked Data

• dbSNP Id: rs528860800
• gnomAD v2: 3-72315831-A-G
• gnomAD v3: 3-72266680-A-G
• gnomAD v4: 3-72266680-A-G
• MyVariant Identifiers: chr3:g.72315831A>G (hg19) ; chr3:g.72266680A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.72266680A>G , CM000665.2:g.72266680A>G	GRCh38
NC_000003.11:g.72315831A>G , CM000665.1:g.72315831A>G	GRCh37
NC_000003.10:g.72398521A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940958.1:n.835+8428T>C