Canonical Allele Identifier: CA1758182929
Gene: LINC03021 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649425G= , CM000670.2:g.2649425G= GRCh38
NC_000008.10:g.2506942G= , CM000670.1:g.2506942G= GRCh37
NC_000008.9:g.2494349G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25305C=