Canonical Allele Identifier: CA16602246

Gene:

Linked Data

• ClinVar Variation Id: 38636
• ClinVar RCV Id: RCV000417226 ; RCV000709915
• MyVariant Identifiers: chr16:g.223300_227103del (hg19) ; chr16:g.173301_177104del (hg38)
• PubMed: PMID:20301608

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173384_177187del , CM000678.2:g.173384_177187del	GRCh38
NC_000016.9:g.223383_227186del , CM000678.1:g.223383_227186del	GRCh37
NC_000016.8:g.163383_167186del	NCBI36
NG_000006.1:g.34247_38050del
NG_059186.1:g.1734_5537del