Canonical Allele Identifier: CA2503076461
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811549G>A , CM000679.2:g.73811549G>A GRCh38
NC_000017.10:g.71807688G>A , CM000679.1:g.71807688G>A GRCh37
NC_000017.9:g.69319283G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12139C>T