Canonical Allele Identifier: CA2104288190
Gene: LINC00331 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836489T= , CM000675.2:g.78836489T= GRCh38
NC_000013.10:g.79410624T= , CM000675.1:g.79410624T= GRCh37
NC_000013.9:g.78308625T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3451A=