Canonical Allele Identifier: CA253224629
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs985993272

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836343C>T , CM000675.2:g.78836343C>T GRCh38
NC_000013.10:g.79410478C>T , CM000675.1:g.79410478C>T GRCh37
NC_000013.9:g.78308479C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3597G>A