Canonical Allele Identifier: CA2274723149
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811591C= , CM000679.2:g.73811591C= GRCh38
NC_000017.10:g.71807730C= , CM000679.1:g.71807730C= GRCh37
NC_000017.9:g.69319325C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12097G=