Canonical Allele Identifier: CA591716263

Gene:

Linked Data

• dbSNP Id: rs1564340095
• gnomAD v2: 10-8739391-A-G
• gnomAD v3: 10-8697428-A-G
• gnomAD v4: 10-8697428-A-G
• MyVariant Identifiers: chr10:g.8739391_8739392delinsGT (hg19) ; chr10:g.8697428_8697429delinsGT (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27627T>C