Canonical Allele Identifier: CA2104288193
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1880408021

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836489_78836490insAGAGG , CM000675.2:g.78836489_78836490insAGAGG GRCh38
NC_000013.10:g.79410624_79410625insAGAGG , CM000675.1:g.79410624_79410625insAGAGG GRCh37
NC_000013.9:g.78308625_78308626insAGAGG NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3450_111+3451insCCTCT