Canonical Allele Identifier: CA913855615
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1566341731

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836399A>G , CM000675.2:g.78836399A>G GRCh38
NC_000013.10:g.79410534A>G , CM000675.1:g.79410534A>G GRCh37
NC_000013.9:g.78308535A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3541T>C