Canonical Allele Identifier: CA2734039702
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs2143599715

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811615G>A , CM000679.2:g.73811615G>A GRCh38
NC_000017.10:g.71807754G>A , CM000679.1:g.71807754G>A GRCh37
NC_000017.9:g.69319349G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12073C>T