Canonical Allele Identifier: CA13888934
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs9574309

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78807966T>C , CM000675.2:g.78807966T>C GRCh38
NC_000013.10:g.79382101T>C , CM000675.1:g.79382101T>C GRCh37
NC_000013.9:g.78280102T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.225-15664A>G