Canonical Allele Identifier: CA51878280
Gene:

Linked Data

dbSNP Id: rs766718895
gnomAD v2: 2-88315659-C-CT
gnomAD v3: 2-88016140-C-CT
gnomAD v4: 2-88016140-C-CT
MyVariant Identifiers: chr2:g.88315662_88315663delinsTGA (hg19) chr2:g.88315659_88315660insT (hg19) chr2:g.88016143_88016144delinsTGA (hg38) chr2:g.88016140_88016141insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016142dup , CM000664.2:g.88016142dup GRCh38
NC_000002.11:g.88315661dup , CM000664.1:g.88315661dup GRCh37
NC_000002.10:g.88096776dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.487dup
XR_940336.3:n.487dup
Search 100 bp 5'
Search 100 bp 3'