Canonical Allele Identifier: CA275015072

Gene:

Linked Data

• dbSNP Id: rs774899037
• MyVariant Identifiers: chr15:g.87962528del (hg19) ; chr15:g.87419297del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419298del , CM000677.2:g.87419298del	GRCh38
NC_000015.9:g.87962529del , CM000677.1:g.87962529del	GRCh37
NC_000015.8:g.85763533del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-26del
XR_932585.1:n.340-26del
XR_001751647.1:n.617-26del
XR_932585.2:n.627-26del