Canonical Allele Identifier: CA584995117
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1455352021
gnomAD v2: 8-126540114-G-A
gnomAD v3: 8-125527872-G-A
gnomAD v4: 8-125527872-G-A
MyVariant Identifiers: chr8:g.126540114G>A (hg19) chr8:g.125527872G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527872G>A , CM000670.2:g.125527872G>A GRCh38
NC_000008.10:g.126540114G>A , CM000670.1:g.126540114G>A GRCh37
NC_000008.9:g.126609296G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54558G>A
XR_001746072.1:n.583+4859G>A
XR_001746073.1:n.583+4859G>A
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