Canonical Allele Identifier: CA862568272

Gene:

Linked Data

• dbSNP Id: rs1445267227
• MyVariant Identifiers: chr9:g.25551523_25551526del (hg19) ; chr9:g.25551525_25551528del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551529_25551532del , CM000671.2:g.25551529_25551532del	GRCh38
NC_000009.11:g.25551527_25551530del , CM000671.1:g.25551527_25551530del	GRCh37
NC_000009.10:g.25541527_25541530del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-956_50-953del
XR_929525.2:n.674-956_674-953del