Canonical Allele Identifier: CA846958447
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1304939298
gnomAD v3: 8-125527537-C-A
gnomAD v4: 8-125527537-C-A
MyVariant Identifiers: chr8:g.126539779C>A (hg19) chr8:g.125527537C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527537C>A , CM000670.2:g.125527537C>A GRCh38
NC_000008.10:g.126539779C>A , CM000670.1:g.126539779C>A GRCh37
NC_000008.9:g.126608961C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54223C>A
XR_001746072.1:n.583+4524C>A
XR_001746073.1:n.583+4524C>A
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