Canonical Allele Identifier: CA2739274963

Gene:

Linked Data

• ClinVar Variation Id: 2902757
• ClinVar RCV Id: RCV003651474

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707335del , CM000667.2:g.112707335del	GRCh38
NC_000005.9:g.112043032del , CM000667.1:g.112043032del	GRCh37
NC_000005.8:g.112070931del	NCBI36
NG_008481.4:g.19815del , LRG_130:g.19815del