Canonical Allele Identifier: CA957924150
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1213345971

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836505G>T , CM000675.2:g.78836505G>T GRCh38
NC_000013.10:g.79410640G>T , CM000675.1:g.79410640G>T GRCh37
NC_000013.9:g.78308641G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3435C>A