Canonical Allele Identifier: CA2274723161
Gene: LINC00469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811623A= , CM000679.2:g.73811623A= GRCh38
NC_000017.10:g.71807762A= , CM000679.1:g.71807762A= GRCh37
NC_000017.9:g.69319357A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12065T=