Canonical Allele Identifier: CA850291575
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1393451997
MyVariant Identifiers: chr8:g.2506680A>T (hg19) chr8:g.2649163A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649163A>T , CM000670.2:g.2649163A>T GRCh38
NC_000008.10:g.2506680A>T , CM000670.1:g.2506680A>T GRCh37
NC_000008.9:g.2494087A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25567T>A
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