Canonical Allele Identifier: CA2104288257
Gene: LINC00331 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836522T= , CM000675.2:g.78836522T= GRCh38
NC_000013.10:g.79410657T= , CM000675.1:g.79410657T= GRCh37
NC_000013.9:g.78308658T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3418A=