Canonical Allele Identifier: CA51878242
Gene:

Linked Data

dbSNP Id: rs368615297
gnomAD v2: 2-88315473-CCAAA-C
gnomAD v3: 2-88015954-CCAAA-C
gnomAD v4: 2-88015954-CCAAA-C
MyVariant Identifiers: chr2:g.88315474_88315477del (hg19) chr2:g.88015955_88015958del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015959_88015962del , CM000664.2:g.88015959_88015962del GRCh38
NC_000002.11:g.88315478_88315481del , CM000664.1:g.88315478_88315481del GRCh37
NC_000002.10:g.88096593_88096596del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.304_307del
XR_940336.3:n.304_307del
Search 100 bp 5'
Search 100 bp 3'