Canonical Allele Identifier: CA716729254

Gene:

Linked Data

• dbSNP Id: rs1400254646
• gnomAD v3: 15-87419362-AC-A
• gnomAD v4: 15-87419362-AC-A
• MyVariant Identifiers: chr15:g.87962594del (hg19) ; chr15:g.87419363del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419363del , CM000677.2:g.87419363del	GRCh38
NC_000015.9:g.87962594del , CM000677.1:g.87962594del	GRCh37
NC_000015.8:g.85763598del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-92del
XR_932585.1:n.340-92del
XR_001751647.1:n.617-92del
XR_932585.2:n.627-92del