Canonical Allele Identifier: CA896967430

Gene:

Linked Data

• dbSNP Id: rs1366084515
• gnomAD v3: 3-109743625-G-A
• gnomAD v4: 3-109743625-G-A
• MyVariant Identifiers: chr3:g.109462472G>A (hg19) ; chr3:g.109743625G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743625G>A , CM000665.2:g.109743625G>A	GRCh38
NC_000003.11:g.109462472G>A , CM000665.1:g.109462472G>A	GRCh37
NC_000003.10:g.110945162G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_924325.1:n.142+63430G>A