Canonical Allele Identifier: CA911527603
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1343655112
gnomAD v3: 3-86495404-T-C
gnomAD v4: 3-86495404-T-C
MyVariant Identifiers: chr3:g.86544554T>C (hg19) chr3:g.86495404T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495404T>C , CM000665.2:g.86495404T>C GRCh38
NC_000003.11:g.86544554T>C , CM000665.1:g.86544554T>C GRCh37
NC_000003.10:g.86627244T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-387T>C
NR_135563.1:n.116-387T>C
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