Canonical Allele Identifier: CA591716262

Gene:

Linked Data

• dbSNP Id: rs1261361636
• gnomAD v2: 10-8739390-GA-G
• gnomAD v3: 10-8697427-GA-G
• gnomAD v4: 10-8697427-GA-G
• MyVariant Identifiers: chr10:g.8739391del (hg19) ; chr10:g.8697428del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697428del , CM000672.2:g.8697428del	GRCh38
NC_000010.10:g.8739391del , CM000672.1:g.8739391del	GRCh37
NC_000010.9:g.8779397del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27627del