Canonical Allele Identifier: CA1846127778

Gene:

Linked Data

• ClinVar Variation Id: 1023948
• ClinVar RCV Id: RCV001324067
• dbSNP Id: rs1823655436

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658074_35658076del , CM000671.2:g.35658074_35658076del	GRCh38
NC_000009.11:g.35658071_35658073del , CM000671.1:g.35658071_35658073del	GRCh37
NC_000009.10:g.35648071_35648073del	NCBI36
NG_017041.1:g.4945_4947del , LRG_163:g.4945_4947del
NG_033120.1:g.4785_4787del