Canonical Allele Identifier: CA1758182930
Gene: LINC03021 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649430A= , CM000670.2:g.2649430A= GRCh38
NC_000008.10:g.2506947A= , CM000670.1:g.2506947A= GRCh37
NC_000008.9:g.2494354A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25300T=