Canonical Allele Identifier: CA170532302
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs983570632
MyVariant Identifiers: chr8:g.2506986A>T (hg19) chr8:g.2649469A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649469A>T , CM000670.2:g.2649469A>T GRCh38
NC_000008.10:g.2506986A>T , CM000670.1:g.2506986A>T GRCh37
NC_000008.9:g.2494393A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25261T>A
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