Canonical Allele Identifier: CA1758182800
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs111870025

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649198G>A , CM000670.2:g.2649198G>A GRCh38
NC_000008.10:g.2506715G>A , CM000670.1:g.2506715G>A GRCh37
NC_000008.9:g.2494122G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25532C>T