Canonical Allele Identifier: CA716729238

Gene:

Linked Data

• dbSNP Id: rs1343980104
• gnomAD v3: 15-87419327-TC-T
• gnomAD v4: 15-87419327-TC-T
• MyVariant Identifiers: chr15:g.87962559del (hg19) ; chr15:g.87419328del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419329del , CM000677.2:g.87419329del	GRCh38
NC_000015.9:g.87962560del , CM000677.1:g.87962560del	GRCh37
NC_000015.8:g.85763564del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-57del
XR_932585.1:n.340-57del
XR_001751647.1:n.617-57del
XR_932585.2:n.627-57del