Canonical Allele Identifier: CA2274723183
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs2047489015
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811661C>G , CM000679.2:g.73811661C>G GRCh38
NC_000017.10:g.71807800C>G , CM000679.1:g.71807800C>G GRCh37
NC_000017.9:g.69319395C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027146.1:n.228+12027G>C
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