Canonical Allele Identifier: CA862567986

Gene:

Linked Data

• dbSNP Id: rs1222519281
• MyVariant Identifiers: chr9:g.25551147_25551152del (hg19) ; chr9:g.25551149_25551154del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551152_25551157del , CM000671.2:g.25551152_25551157del	GRCh38
NC_000009.11:g.25551150_25551155del , CM000671.1:g.25551150_25551155del	GRCh37
NC_000009.10:g.25541150_25541155del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-582_50-577del
XR_929525.2:n.674-582_674-577del