Canonical Allele Identifier: CA2104288279
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1880409070
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836559G>A , CM000675.2:g.78836559G>A GRCh38
NC_000013.10:g.79410694G>A , CM000675.1:g.79410694G>A GRCh37
NC_000013.9:g.78308695G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3381C>T
Search 100 bp 5'
Search 100 bp 3'