Canonical Allele Identifier: CA259818

Gene:

Linked Data

• ClinVar Variation Id: 30441
• ClinVar RCV Id: RCV000023394
• MyVariant Identifiers: chr1:g.45794768_45799052delinsTA (hg19) ; chr1:g.45329096_45333380delinsTA (hg38)
• PubMed: PMID:21815886 ; PMID:23035301

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45329096_45333380delinsTA , CM000663.2:g.45329096_45333380delinsTA	GRCh38
NC_000001.10:g.45794768_45799052delinsTA , CM000663.1:g.45794768_45799052delinsTA	GRCh37
NC_000001.9:g.45567355_45571639delinsTA	NCBI36
NG_008189.1:g.12091_16375delinsTA , LRG_220:g.12091_16375delinsTA