Canonical Allele Identifier: CA2274723038
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs2047487204
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811400C>A , CM000679.2:g.73811400C>A GRCh38
NC_000017.10:g.71807539C>A , CM000679.1:g.71807539C>A GRCh37
NC_000017.9:g.69319134C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12288G>T
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