Canonical Allele Identifier: CA656870453
Gene: LINC00469 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811547G>T , CM000679.2:g.73811547G>T GRCh38
NC_000017.10:g.71807686G>T , CM000679.1:g.71807686G>T GRCh37
NC_000017.9:g.69319281G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12141C>A