Canonical Allele Identifier: CA294608039
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs964151947
MyVariant Identifiers: chr17:g.71807775G>C (hg19) chr17:g.73811636G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811636G>C , CM000679.2:g.73811636G>C GRCh38
NC_000017.10:g.71807775G>C , CM000679.1:g.71807775G>C GRCh37
NC_000017.9:g.69319370G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12052C>G
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