Canonical Allele Identifier: CA957924139
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1880407508

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836457T>C , CM000675.2:g.78836457T>C GRCh38
NC_000013.10:g.79410592T>C , CM000675.1:g.79410592T>C GRCh37
NC_000013.9:g.78308593T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3483A>G