Canonical Allele Identifier: CA894254470

Gene:

Linked Data

• dbSNP Id: rs1293401562
• gnomAD v3: 2-88016264-G-GT
• gnomAD v4: 2-88016264-G-GT
• MyVariant Identifiers: chr2:g.88315783_88315784insT (hg19) ; chr2:g.88016264_88016265insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016270dup , CM000664.2:g.88016270dup	GRCh38
NC_000002.11:g.88315789dup , CM000664.1:g.88315789dup	GRCh37
NC_000002.10:g.88096904dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.615dup
XR_940336.3:n.615dup