Canonical Allele Identifier: CA294608019
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs375690674

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811521G>A , CM000679.2:g.73811521G>A GRCh38
NC_000017.10:g.71807660G>A , CM000679.1:g.71807660G>A GRCh37
NC_000017.9:g.69319255G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12167C>T