Canonical Allele Identifier: CA2274723061
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs2047487438
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811435G>A , CM000679.2:g.73811435G>A GRCh38
NC_000017.10:g.71807574G>A , CM000679.1:g.71807574G>A GRCh37
NC_000017.9:g.69319169G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027146.1:n.228+12253C>T
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Search 100 bp 3'