Canonical Allele Identifier: CA534638435

Gene:

Linked Data

• gnomAD v2: 2-88315790-CTTCTTTA-C
• MyVariant Identifiers: chr2:g.88315791_88315797del (hg19) ; chr2:g.88016272_88016278del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016272_88016278del , CM000664.2:g.88016272_88016278del	GRCh38
NC_000002.11:g.88315791_88315797del , CM000664.1:g.88315791_88315797del	GRCh37
NC_000002.10:g.88096906_88096912del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.617_623del
XR_940336.3:n.617_623del