Canonical Allele Identifier: CA894242679

Gene:

Linked Data

• dbSNP Id: rs1196499928
• gnomAD v3: 2-88016414-TAAACTC-T
• gnomAD v4: 2-88016414-TAAACTC-T
• MyVariant Identifiers: chr2:g.88315934_88315939del (hg19) ; chr2:g.88016415_88016420del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016415_88016420del , CM000664.2:g.88016415_88016420del	GRCh38
NC_000002.11:g.88315934_88315939del , CM000664.1:g.88315934_88315939del	GRCh37
NC_000002.10:g.88097049_88097054del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.760_765del
XR_940336.3:n.760_765del