Canonical Allele Identifier: CA658821623
Gene:

Linked Data

ClinVar Variation Id: 551791
dbSNP Id: rs1554651600
MyVariant Identifiers: chr9:g.35658073del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658073del , CM000671.2:g.35658073del GRCh38
NC_000009.11:g.35658070del , CM000671.1:g.35658070del GRCh37
NC_000009.10:g.35648070del NCBI36
NG_017041.1:g.4946del , LRG_163:g.4946del
NG_033120.1:g.4784del