Canonical Allele Identifier: CA2598022253
Gene: LINC00469 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811542A>T , CM000679.2:g.73811542A>T GRCh38
NC_000017.10:g.71807681A>T , CM000679.1:g.71807681A>T GRCh37
NC_000017.9:g.69319276A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12146T>A