Canonical Allele Identifier: CA212478

Gene:

Linked Data

• ClinVar Variation Id: 157440
• ClinVar RCV Id: RCV000161866
• MyVariant Identifiers: chr19:g.35587635_35597215del (hg19) ; chr19:g.35096731_35106311del (hg38)
• PubMed: PMID:25666259

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35096731_35106311del , CM000681.2:g.35096731_35106311del	GRCh38
NC_000019.9:g.35587635_35597215del , CM000681.1:g.35587635_35597215del	GRCh37
NC_000019.8:g.40279475_40289055del	NCBI36