Canonical Allele Identifier: CA185516649
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs561899318
gnomAD v3: 8-125527673-C-T
gnomAD v4: 8-125527673-C-T
MyVariant Identifiers: chr8:g.126539915C>T (hg19) chr8:g.125527673C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527673C>T , CM000670.2:g.125527673C>T GRCh38
NC_000008.10:g.126539915C>T , CM000670.1:g.126539915C>T GRCh37
NC_000008.9:g.126609097C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54359C>T
XR_001746072.1:n.583+4660C>T
XR_001746073.1:n.583+4660C>T
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