Canonical Allele Identifier: CA534498801

Gene:

Linked Data

• dbSNP Id: rs1472504932
• gnomAD v2: 2-88315391-GGTGAGGATC-G
• gnomAD v3: 2-88015872-GGTGAGGATC-G
• gnomAD v4: 2-88015872-GGTGAGGATC-G
• MyVariant Identifiers: chr2:g.88315392_88315400del (hg19) ; chr2:g.88015873_88015881del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88015874_88015882del , CM000664.2:g.88015874_88015882del	GRCh38
NC_000002.11:g.88315393_88315401del , CM000664.1:g.88315393_88315401del	GRCh37
NC_000002.10:g.88096508_88096516del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.219_227del
XR_940336.3:n.219_227del