Canonical Allele Identifier: CA916083168
Gene:

Linked Data

ClinVar Variation Id: 869247
ClinVar RCV Id: RCV001078282

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225158_5227199delinsCTTAT , CM000673.2:g.5225158_5227199delinsCTTAT GRCh38
NC_000011.9:g.5246388_5248429delinsCTTAT , CM000673.1:g.5246388_5248429delinsCTTAT GRCh37
NC_000011.8:g.5202964_5205005delinsCTTAT NCBI36
NG_000007.3:g.70417_72458delinsATAAG
NG_059281.1:g.4873_6914delinsATAAG