Canonical Allele Identifier: CA170532299
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1006902544
MyVariant Identifiers: chr8:g.2506932A>G (hg19) chr8:g.2649415A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649415A>G , CM000670.2:g.2649415A>G GRCh38
NC_000008.10:g.2506932A>G , CM000670.1:g.2506932A>G GRCh37
NC_000008.9:g.2494339A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25315T>C
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