Canonical Allele Identifier: CA1758182952
Gene: LINC03021 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649480G= , CM000670.2:g.2649480G= GRCh38
NC_000008.10:g.2506997G= , CM000670.1:g.2506997G= GRCh37
NC_000008.9:g.2494404G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25250C=