Canonical Allele Identifier: CA2104288269
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1880408946

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836552C>A , CM000675.2:g.78836552C>A GRCh38
NC_000013.10:g.79410687C>A , CM000675.1:g.79410687C>A GRCh37
NC_000013.9:g.78308688C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3388G>T