Canonical Allele Identifier: CA2499216341

Gene:

Linked Data

• ClinVar Variation Id: 997743
• ClinVar RCV Id: RCV001293300

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10137102_10143357del , CM000665.2:g.10137102_10143357del	GRCh38
NC_000003.11:g.10178786_10185041del , CM000665.1:g.10178786_10185041del	GRCh37
NC_000003.10:g.10153786_10160041del	NCBI36
NG_008212.3:g.468_6723del , LRG_322:g.468_6723del