Canonical Allele Identifier: CA340268

Gene:

Linked Data

• ClinVar Variation Id: 4608
• ClinVar RCV Id: RCV000004871
• MyVariant Identifiers: chr3:g.148844501_148848419del (hg19) ; chr3:g.149126714_149130632del (hg38)
• PubMed: PMID:11455388 ; PMID:11590544 ; PMID:20301464

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149126714_149130632del , CM000665.2:g.149126714_149130632del	GRCh38
NC_000003.11:g.148844501_148848419del , CM000665.1:g.148844501_148848419del	GRCh37
NC_000003.10:g.150327191_150331109del	NCBI36
NG_009847.1:g.2131_6049del