Canonical Allele Identifier: CA2274723152
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811594T= , CM000679.2:g.73811594T= GRCh38
NC_000017.10:g.71807733T= , CM000679.1:g.71807733T= GRCh37
NC_000017.9:g.69319328T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12094A=