Canonical Allele Identifier: CA957924073
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1880405280

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836346_78836373del , CM000675.2:g.78836346_78836373del GRCh38
NC_000013.10:g.79410481_79410508del , CM000675.1:g.79410481_79410508del GRCh37
NC_000013.9:g.78308482_78308509del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3576_111+3603del