Canonical Allele Identifier: CA638953170
Gene:

Linked Data

ClinVar Variation Id: 1266304
ClinVar RCV Id: RCV001676127
dbSNP Id: rs374222410

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.25231931_25231932del , CM000684.2:g.25231931_25231932del GRCh38
NC_000022.10:g.25627898_25627899del , CM000684.1:g.25627898_25627899del GRCh37
NC_000022.9:g.23957898_23957899del NCBI36
NG_009827.1:g.17287_17288del