Canonical Allele Identifier: CA51878264
Gene:

Linked Data

dbSNP Id: rs906765828
gnomAD v3: 2-88016075-CAGTG-C
gnomAD v4: 2-88016075-CAGTG-C
MyVariant Identifiers: chr2:g.88315595_88315598del (hg19) chr2:g.88016076_88016079del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016079_88016082del , CM000664.2:g.88016079_88016082del GRCh38
NC_000002.11:g.88315598_88315601del , CM000664.1:g.88315598_88315601del GRCh37
NC_000002.10:g.88096713_88096716del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.424_427del
XR_940336.3:n.424_427del
Search 100 bp 5'
Search 100 bp 3'