Canonical Allele Identifier: CA2274723037
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811391T= , CM000679.2:g.73811391T= GRCh38
NC_000017.10:g.71807530T= , CM000679.1:g.71807530T= GRCh37
NC_000017.9:g.69319125T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12297A=