Canonical Allele Identifier: CA916083178

Gene:

Linked Data

• ClinVar Variation Id: 38702
• ClinVar RCV Id: RCV001078287

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226164_5227556del , CM000673.2:g.5226164_5227556del	GRCh38
NC_000011.9:g.5247394_5248786del , CM000673.1:g.5247394_5248786del	GRCh37
NC_000011.8:g.5203970_5205362del	NCBI36
NG_000007.3:g.70061_71453del
NG_059281.1:g.4517_5909del