Canonical Allele Identifier: CA63882912
Gene:

Linked Data

ClinVar Variation Id: 7763
ClinVar RCV Id: RCV000008204
dbSNP Id: rs3834129

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201232809_201232814del , CM000664.2:g.201232809_201232814del GRCh38
NC_000002.11:g.202097532_202097537del , CM000664.1:g.202097532_202097537del GRCh37
NC_000002.10:g.201805777_201805782del NCBI36
NG_007497.1:g.4352_4357del , LRG_34:g.4352_4357del