Canonical Allele Identifier: CA915942366

Gene:

Linked Data

• ClinVar Variation Id: 812937
• ClinVar RCV Id: RCV001003873

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202373247_202381017del , CM000664.2:g.202373247_202381017del	GRCh38
NC_000002.11:g.203237970_203245740del , CM000664.1:g.203237970_203245740del	GRCh37
NC_000002.10:g.202946215_202953985del	NCBI36
NG_009363.1:g.1921_9691del , LRG_712:g.1921_9691del