Canonical Allele Identifier: CA591716259

Gene:

Linked Data

• dbSNP Id: rs1285496561
• gnomAD v2: 10-8739352-A-G
• gnomAD v3: 10-8697389-A-G
• gnomAD v4: 10-8697389-A-G
• MyVariant Identifiers: chr10:g.8739352A>G (hg19) ; chr10:g.8697389A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697389A>G , CM000672.2:g.8697389A>G	GRCh38
NC_000010.10:g.8739352A>G , CM000672.1:g.8739352A>G	GRCh37
NC_000010.9:g.8779358A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27588T>C