Canonical Allele Identifier: CA2534717959
Gene: LINC00880 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119106G>T , CM000665.2:g.157119106G>T GRCh38
NC_000003.11:g.156836895G>T , CM000665.1:g.156836895G>T GRCh37
NC_000003.10:g.158319589G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3770C>A
Search 100 bp 5'
Search 100 bp 3'