Canonical Allele Identifier: CA462884051
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1302599153
gnomAD v3: 8-125527701-C-T
gnomAD v4: 8-125527701-C-T
MyVariant Identifiers: chr8:g.126539943C>T (hg19) chr8:g.125527701C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527701C>T , CM000670.2:g.125527701C>T GRCh38
NC_000008.10:g.126539943C>T , CM000670.1:g.126539943C>T GRCh37
NC_000008.9:g.126609125C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54387C>T
XR_001746072.1:n.583+4688C>T
XR_001746073.1:n.583+4688C>T
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