Canonical Allele Identifier: CA202788766

Gene:

Linked Data

• dbSNP Id: rs138858818
• gnomAD v2: 10-8739384-CTA-C
• gnomAD v3: 10-8697421-CTA-C
• gnomAD v4: 10-8697421-CTA-C
• MyVariant Identifiers: chr10:g.8739385_8739386del (hg19) ; chr10:g.8697422_8697423del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697423_8697424del , CM000672.2:g.8697423_8697424del	GRCh38
NC_000010.10:g.8739386_8739387del , CM000672.1:g.8739386_8739387del	GRCh37
NC_000010.9:g.8779392_8779393del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27622_33-27621del