Canonical Allele Identifier: CA2598935841
Gene: LINC02254 HGNC NCBI
LINC02253 HGNC NCBI

Linked Data

dbSNP Id: rs1898055441
gnomAD v3: 15-97396131-C-G
gnomAD v4: 15-97396131-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97396131C>G , CM000677.2:g.97396131C>G GRCh38
NC_000015.9:g.97939361C>G , CM000677.1:g.97939361C>G GRCh37
NC_000015.8:g.95740365C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120324.1:n.755+1526G>C (LINC02254)
XR_001751693.1:n.305-15061C>G (LINC02253)
XR_001751694.1:n.305-15061C>G (LINC02253)
XR_001751695.1:n.305-15061C>G (LINC02253)
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