Canonical Allele Identifier: CA1573442159
Gene:

Linked Data

ClinVar Variation Id: 1063913
ClinVar RCV Id: RCV003652231
dbSNP Id: rs1750548511

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707331_112707355dup , CM000667.2:g.112707331_112707355dup GRCh38
NC_000005.9:g.112043028_112043052dup , CM000667.1:g.112043028_112043052dup GRCh37
NC_000005.8:g.112070927_112070951dup NCBI36
NG_008481.4:g.19811_19835dup , LRG_130:g.19811_19835dup