Canonical Allele Identifier: CA339677

Gene:

Linked Data

• ClinVar Variation Id: 219074
• ClinVar RCV Id: RCV000203460
• MyVariant Identifiers: chr2:g.32288217_32292251del (hg19) ; chr2:g.32063148_32067182del (hg38)
• PubMed: PMID:25065914

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32063148_32067182del , CM000664.2:g.32063148_32067182del	GRCh38
NC_000002.11:g.32288217_32292251del , CM000664.1:g.32288217_32292251del	GRCh37
NC_000002.10:g.32141721_32145755del	NCBI36
NG_008730.1:g.4538_8572del , LRG_714:g.4538_8572del