Canonical Allele Identifier: CA619736677

Gene:

Linked Data

• dbSNP Id: rs1217294592
• gnomAD v2: 15-87962524-AGG-A
• gnomAD v3: 15-87419293-AGG-A
• gnomAD v4: 15-87419293-AGG-A
• MyVariant Identifiers: chr15:g.87962525_87962526del (hg19) ; chr15:g.87419294_87419295del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419294_87419295del , CM000677.2:g.87419294_87419295del	GRCh38
NC_000015.9:g.87962525_87962526del , CM000677.1:g.87962525_87962526del	GRCh37
NC_000015.8:g.85763529_85763530del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-24_340-23del
XR_932585.1:n.340-24_340-23del
XR_001751647.1:n.617-24_617-23del
XR_932585.2:n.627-24_627-23del