Canonical Allele Identifier: CA2350433810
Gene: LINC00687 HGNC NCBI

Linked Data

dbSNP Id: rs1159515498
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810021A>T , CM000682.2:g.11810021A>T GRCh38
NC_000020.10:g.11790669A>T , CM000682.1:g.11790669A>T GRCh37
NC_000020.9:g.11738669A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110635.1:n.490T>A
Search 100 bp 5'
Search 100 bp 3'