Canonical Allele Identifier: CA77246671

Gene:

Linked Data

• dbSNP Id: rs56217453
• gnomAD v2: 3-72315970-AACACACACACACACAC-A
• gnomAD v3: 3-72266819-AACACACACACACACAC-A
• gnomAD v4: 3-72266819-AACACACACACACACAC-A
• MyVariant Identifiers: chr3:g.72315971_72315986del (hg19) ; chr3:g.72266820_72266835del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.72266856_72266871del , CM000665.2:g.72266856_72266871del	GRCh38
NC_000003.11:g.72316007_72316022del , CM000665.1:g.72316007_72316022del	GRCh37
NC_000003.10:g.72398697_72398712del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940958.1:n.835+8273_835+8288del