Canonical Allele Identifier: CA2799837012
Gene: LINC00331 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836661C>G , CM000675.2:g.78836661C>G GRCh38
NC_000013.10:g.79410796C>G , CM000675.1:g.79410796C>G GRCh37
NC_000013.9:g.78308797C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3279G>C