Canonical Allele Identifier: CA620039571
Gene: LINC02254 HGNC NCBI
LINC02253 HGNC NCBI

Linked Data

dbSNP Id: rs1346053744
gnomAD v2: 15-97939264-T-A
gnomAD v3: 15-97396034-T-A
gnomAD v4: 15-97396034-T-A
MyVariant Identifiers: chr15:g.97939264T>A (hg19) chr15:g.97396034T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97396034T>A , CM000677.2:g.97396034T>A GRCh38
NC_000015.9:g.97939264T>A , CM000677.1:g.97939264T>A GRCh37
NC_000015.8:g.95740268T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120324.1:n.755+1623A>T (LINC02254)
XR_001751693.1:n.305-15158T>A (LINC02253)
XR_001751694.1:n.305-15158T>A (LINC02253)
XR_001751695.1:n.305-15158T>A (LINC02253)
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