Canonical Allele Identifier: CA894242558
Gene:

Linked Data

dbSNP Id: rs1316890253
gnomAD v3: 2-88016393-C-CGATGCGTAGACTA
gnomAD v4: 2-88016393-C-CGATGCGTAGACTA
MyVariant Identifiers: chr2:g.88315912_88315913insGATGCGTAGACTA (hg19) chr2:g.88016393_88016394insGATGCGTAGACTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016397_88016409dup , CM000664.2:g.88016397_88016409dup GRCh38
NC_000002.11:g.88315916_88315928dup , CM000664.1:g.88315916_88315928dup GRCh37
NC_000002.10:g.88097031_88097043dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.742_754dup
XR_940336.3:n.742_754dup
Search 100 bp 5'
Search 100 bp 3'