Canonical Allele Identifier: CA185516664
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs761743186
gnomAD v2: 8-126540048-T-C
gnomAD v3: 8-125527806-T-C
gnomAD v4: 8-125527806-T-C
MyVariant Identifiers: chr8:g.126540048T>C (hg19) chr8:g.125527806T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527806T>C , CM000670.2:g.125527806T>C GRCh38
NC_000008.10:g.126540048T>C , CM000670.1:g.126540048T>C GRCh37
NC_000008.9:g.126609230T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54492T>C
XR_001746072.1:n.583+4793T>C
XR_001746073.1:n.583+4793T>C
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