Canonical Allele Identifier: CA797158687

Gene:

Linked Data

• dbSNP Id: rs1212017489
• gnomAD v3: 4-62558237-A-AG
• gnomAD v4: 4-62558237-A-AG
• MyVariant Identifiers: chr4:g.63423955_63423956insG (hg19) ; chr4:g.62558237_62558238insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62558238dup , CM000666.2:g.62558238dup	GRCh38
NC_000004.11:g.63423956dup , CM000666.1:g.63423956dup	GRCh37
NC_000004.10:g.63106551dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938814.1:n.161-5606dup