Canonical Allele Identifier: CA2104288075
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1880406703

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836400A>G , CM000675.2:g.78836400A>G GRCh38
NC_000013.10:g.79410535A>G , CM000675.1:g.79410535A>G GRCh37
NC_000013.9:g.78308536A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3540T>C