Canonical Allele Identifier: CA2274723187
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811671G= , CM000679.2:g.73811671G= GRCh38
NC_000017.10:g.71807810G= , CM000679.1:g.71807810G= GRCh37
NC_000017.9:g.69319405G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12017C=