Canonical Allele Identifier: CA16042153
Gene:

Linked Data

ClinVar Variation Id: 371894
dbSNP Id: rs5030658

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737128del , CM000678.2:g.68737128del GRCh38
NC_000016.9:g.68771031del , CM000678.1:g.68771031del GRCh37
NC_000016.8:g.67328532del NCBI36
NG_008021.1:g.4837del , LRG_301:g.4837del