Canonical Allele Identifier: CA1758182934
Gene: LINC03021 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649433C= , CM000670.2:g.2649433C= GRCh38
NC_000008.10:g.2506950C= , CM000670.1:g.2506950C= GRCh37
NC_000008.9:g.2494357C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25297G=