Canonical Allele Identifier: CA544492009
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1559599501
gnomAD v2: 3-86544387-GTGTGTGT-G
gnomAD v3: 3-86495237-GTGTGTGT-G
gnomAD v4: 3-86495237-GTGTGTGT-G
MyVariant Identifiers: chr3:g.86544388_86544402delinsGTGTGTGT (hg19) chr3:g.86495238_86495252delinsGTGTGTGT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495238_86495244del , CM000665.2:g.86495238_86495244del GRCh38
NC_000003.11:g.86544388_86544394del , CM000665.1:g.86544388_86544394del GRCh37
NC_000003.10:g.86627078_86627084del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245082.1:n.116-553_116-547del
NR_135563.1:n.116-553_116-547del
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