Canonical Allele Identifier: CA1758182914
Gene: LINC03021 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649383G= , CM000670.2:g.2649383G= GRCh38
NC_000008.10:g.2506900G= , CM000670.1:g.2506900G= GRCh37
NC_000008.9:g.2494307G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25347C=