Canonical Allele Identifier: CA2499222420
Gene:

Linked Data

ClinVar Variation Id: 1066897
ClinVar RCV Id: RCV001378016
dbSNP Id: rs2138025968

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303714_48303721del , CM000675.2:g.48303714_48303721del GRCh38
NC_000013.10:g.48877850_48877857del , CM000675.1:g.48877850_48877857del GRCh37
NC_000013.9:g.47775851_47775858del NCBI36
NG_009009.1:g.4968_4975del , LRG_517:g.4968_4975del