Canonical Allele Identifier: CA915942297

Gene:

Linked Data

• ClinVar Variation Id: 827699
• ClinVar RCV Id: RCV001027563

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203870597_203875386del , CM000664.2:g.203870597_203875386del	GRCh38
NC_000002.11:g.204735320_204740109del , CM000664.1:g.204735320_204740109del	GRCh37
NC_000002.10:g.204443565_204448354del	NCBI36
NG_011502.1:g.7812_12601del