Canonical Allele Identifier: CA894254733

Gene:

Linked Data

• dbSNP Id: rs1354150171
• gnomAD v3: 2-88016351-GTTAGCAGGTGCAC-G
• gnomAD v4: 2-88016351-GTTAGCAGGTGCAC-G
• MyVariant Identifiers: chr2:g.88315871_88315883del (hg19) ; chr2:g.88016352_88016364del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016352_88016364del , CM000664.2:g.88016352_88016364del	GRCh38
NC_000002.11:g.88315871_88315883del , CM000664.1:g.88315871_88315883del	GRCh37
NC_000002.10:g.88096986_88096998del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.697_709del
XR_940336.3:n.697_709del