Canonical Allele Identifier: CA2274723044
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811407C= , CM000679.2:g.73811407C= GRCh38
NC_000017.10:g.71807546C= , CM000679.1:g.71807546C= GRCh37
NC_000017.9:g.69319141C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027146.1:n.228+12281G=