Canonical Allele Identifier: CA957924079
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1880405582

Genomic Alleles

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

Transcript Alleles

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