Canonical Allele Identifier: CA14425624
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73763821C>T , CM000679.2:g.73763821C>T GRCh38
NC_000017.10:g.71759960C>T , CM000679.1:g.71759960C>T GRCh37
NC_000017.9:g.69271555C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027146.1:n.229-2795G>A