Canonical Allele Identifier: CA170532263
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1003097920
COSMIC: COSN9629268
MyVariant Identifiers: chr8:g.2506726G>A (hg19) chr8:g.2649209G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649209G>A , CM000670.2:g.2649209G>A GRCh38
NC_000008.10:g.2506726G>A , CM000670.1:g.2506726G>A GRCh37
NC_000008.9:g.2494133G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25521C>T
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