Canonical Allele Identifier: CA896967349

Gene:

Linked Data

• dbSNP Id: rs1259443102
• MyVariant Identifiers: chr3:g.109462307A>G (hg19) ; chr3:g.109743460A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743460A>G , CM000665.2:g.109743460A>G	GRCh38
NC_000003.11:g.109462307A>G , CM000665.1:g.109462307A>G	GRCh37
NC_000003.10:g.110944997A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924325.1:n.142+63265A>G