Canonical Allele Identifier: CA627574250
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs1334878145

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811499A>T , CM000679.2:g.73811499A>T GRCh38
NC_000017.10:g.71807638A>T , CM000679.1:g.71807638A>T GRCh37
NC_000017.9:g.69319233A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12189T>A