Canonical Allele Identifier: CA2799837008
Gene: LINC00331 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836449A>T , CM000675.2:g.78836449A>T GRCh38
NC_000013.10:g.79410584A>T , CM000675.1:g.79410584A>T GRCh37
NC_000013.9:g.78308585A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3491T>A