Canonical Allele Identifier: CA10584071
Gene:

Linked Data

ClinVar Variation Id: 243058
ClinVar RCV Id: RCV000235059
MyVariant Identifiers: chr1:g.161275598_161279773dup (hg19) chr1:g.161275598_161279773dup4176 (hg19)
PubMed: PMID:21787890 PMID:26378787
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161305808_161309983dup , CM000663.2:g.161305808_161309983dup GRCh38
NC_000001.10:g.161275598_161279773dup , CM000663.1:g.161275598_161279773dup GRCh37
NC_000001.9:g.159542222_159546397dup NCBI36
NG_008055.1:g.4990_9165dup , LRG_256:g.4990_9165dup
Search 100 bp 5'
Search 100 bp 3'