Canonical Allele Identifier: CA656870455
Gene: LINC00469 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811572A>C , CM000679.2:g.73811572A>C GRCh38
NC_000017.10:g.71807711A>C , CM000679.1:g.71807711A>C GRCh37
NC_000017.9:g.69319306A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12116T>G