Canonical Allele Identifier: CA2104288049
Gene: LINC00331 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836378A= , CM000675.2:g.78836378A= GRCh38
NC_000013.10:g.79410513A= , CM000675.1:g.79410513A= GRCh37
NC_000013.9:g.78308514A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3562T=