Canonical Allele Identifier: CA202788778

Gene:

Linked Data

• dbSNP Id: rs938189967
• gnomAD v3: 10-8697517-A-G
• gnomAD v4: 10-8697517-A-G
• MyVariant Identifiers: chr10:g.8739480A>G (hg19) ; chr10:g.8697517A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697517A>G , CM000672.2:g.8697517A>G	GRCh38
NC_000010.10:g.8739480A>G , CM000672.1:g.8739480A>G	GRCh37
NC_000010.9:g.8779486A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27716T>C