Canonical Allele Identifier: CA986186292
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs2047488549

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811584A>G , CM000679.2:g.73811584A>G GRCh38
NC_000017.10:g.71807723A>G , CM000679.1:g.71807723A>G GRCh37
NC_000017.9:g.69319318A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12104T>C