Canonical Allele Identifier: CA71252402

Gene:

Linked Data

• dbSNP Id: rs779661407
• gnomAD v3: 3-21207084-T-G
• gnomAD v4: 3-21207084-T-G
• MyVariant Identifiers: chr3:g.21248576T>G (hg19) ; chr3:g.21207084T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.21207084T>G , CM000665.2:g.21207084T>G	GRCh38
NC_000003.11:g.21248576T>G , CM000665.1:g.21248576T>G	GRCh37
NC_000003.10:g.21223580T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940646.1:n.254-3914T>G
XR_940646.2:n.547-3914T>G