Canonical Allele Identifier: CA2759045340
Gene: LINC00880 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.157119153C>T , CM000665.2:g.157119153C>T GRCh38
NC_000003.11:g.156836942C>T , CM000665.1:g.156836942C>T GRCh37
NC_000003.10:g.158319636C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_034007.1:n.127+3723G>A