Canonical Allele Identifier: CA537204546
Gene:

Linked Data

dbSNP Id: rs1393484785
gnomAD v2: 2-156727186-G-GGGCAATAGGA
gnomAD v3: 2-155870674-G-GGGCAATAGGA
gnomAD v4: 2-155870674-G-GGGCAATAGGA
MyVariant Identifiers: chr2:g.156727186_156727187insGGCAATAGGA (hg19) chr2:g.155870674_155870675insGGCAATAGGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870674_155870675insGGCAATAGGA , CM000664.2:g.155870674_155870675insGGCAATAGGA GRCh38
NC_000002.11:g.156727186_156727187insGGCAATAGGA , CM000664.1:g.156727186_156727187insGGCAATAGGA GRCh37
NC_000002.10:g.156435432_156435433insGGCAATAGGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3488_320-3487insTCCTATTGCC
XR_001739749.1:n.331-29691_331-29690insTCCTATTGCC
XR_001739750.1:n.331-29691_331-29690insTCCTATTGCC
XR_001739751.1:n.331-29691_331-29690insTCCTATTGCC
XR_923501.2:n.331-3488_331-3487insTCCTATTGCC
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