Canonical Allele Identifier: CA2274723133
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811567C= , CM000679.2:g.73811567C= GRCh38
NC_000017.10:g.71807706C= , CM000679.1:g.71807706C= GRCh37
NC_000017.9:g.69319301C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12121G=