Canonical Allele Identifier: CA1758182758
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1563051312

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649108C>T , CM000670.2:g.2649108C>T GRCh38
NC_000008.10:g.2506625C>T , CM000670.1:g.2506625C>T GRCh37
NC_000008.9:g.2494032C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25622G>A