Canonical Allele Identifier: CA701182672
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1332691550

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836437_78836439del , CM000675.2:g.78836437_78836439del GRCh38
NC_000013.10:g.79410572_79410574del , CM000675.1:g.79410572_79410574del GRCh37
NC_000013.9:g.78308573_78308575del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3505_111+3507del