Canonical Allele Identifier: CA701182689
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1439707147

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836495A>G , CM000675.2:g.78836495A>G GRCh38
NC_000013.10:g.79410630A>G , CM000675.1:g.79410630A>G GRCh37
NC_000013.9:g.78308631A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046869.2:n.111+3445T>C