Canonical Allele Identifier: CA2104288185
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1880407936

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836486_78836490del , CM000675.2:g.78836486_78836490del GRCh38
NC_000013.10:g.79410621_79410625del , CM000675.1:g.79410621_79410625del GRCh37
NC_000013.9:g.78308622_78308626del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3451_111+3455del