Canonical Allele Identifier: CA2104287997
Gene: LINC00331 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836350G= , CM000675.2:g.78836350G= GRCh38
NC_000013.10:g.79410485G= , CM000675.1:g.79410485G= GRCh37
NC_000013.9:g.78308486G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3590C=