Canonical Allele Identifier: CA957924105
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1880406010

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836364del , CM000675.2:g.78836364del GRCh38
NC_000013.10:g.79410499del , CM000675.1:g.79410499del GRCh37
NC_000013.9:g.78308500del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3576del