Canonical Allele Identifier: CA2274723131
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811561A= , CM000679.2:g.73811561A= GRCh38
NC_000017.10:g.71807700A= , CM000679.1:g.71807700A= GRCh37
NC_000017.9:g.69319295A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12127T=