Canonical Allele Identifier: CA894254589

Gene:

Linked Data

• dbSNP Id: rs1217663484
• gnomAD v2: 2-88315820-AG-A
• gnomAD v3: 2-88016301-AG-A
• gnomAD v4: 2-88016301-AG-A
• MyVariant Identifiers: chr2:g.88315821del (hg19) ; chr2:g.88016302del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016302del , CM000664.2:g.88016302del	GRCh38
NC_000002.11:g.88315821del , CM000664.1:g.88315821del	GRCh37
NC_000002.10:g.88096936del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.647del
XR_940336.3:n.647del