Canonical Allele Identifier: CA1026956590
Community Standard Title: NC_000002.12:g.2922241G>C
Gene: LINC01250 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.2922241G>C , CM000664.2:g.2922241G>C GRCh38
NC_000002.11:g.2926013G>C , CM000664.1:g.2926013G>C GRCh37
NC_000002.10:g.2905020G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110228.1:n.595-24937C>G