Canonical Allele Identifier: CA202788776

Gene:

Linked Data

• dbSNP Id: rs141618011
• gnomAD v2: 10-8739462-C-A
• gnomAD v3: 10-8697499-C-A
• gnomAD v4: 10-8697499-C-A
• MyVariant Identifiers: chr10:g.8739462C>A (hg19) ; chr10:g.8697499C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697499C>A , CM000672.2:g.8697499C>A	GRCh38
NC_000010.10:g.8739462C>A , CM000672.1:g.8739462C>A	GRCh37
NC_000010.9:g.8779468C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27698G>T