Canonical Allele Identifier: CA909017119

Gene:

Linked Data

• dbSNP Id: rs1344767309
• gnomAD v3: 3-61428089-GCTTGCTATAAAGAAT-G
• gnomAD v4: 3-61428089-GCTTGCTATAAAGAAT-G
• MyVariant Identifiers: chr3:g.61413764_61413778del (hg19) ; chr3:g.61428090_61428104del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.61428097_61428111del , CM000665.2:g.61428097_61428111del	GRCh38
NC_000003.11:g.61413771_61413785del , CM000665.1:g.61413771_61413785del	GRCh37
NC_000003.10:g.61388811_61388825del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_940892.1:n.164+410_165-404del
XR_940893.1:n.164+410_164+424del
XR_001740725.1:n.202+410_202+424del
XR_940892.2:n.202+410_203-404del