Canonical Allele Identifier: CA1139656915

Gene:

Linked Data

• ClinVar Variation Id: 937627
• ClinVar RCV Id: RCV001206681

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47401748_47403287del , CM000664.2:g.47401748_47403287del	GRCh38
NC_000002.11:g.47628887_47630426del , CM000664.1:g.47628887_47630426del	GRCh37
NC_000002.10:g.47482391_47483930del	NCBI36
NG_007110.2:g.3625_5164del , LRG_218:g.3625_5164del