Canonical Allele Identifier: CA1526083817
Gene: LINC02226 HGNC NCBI

Linked Data

dbSNP Id: rs2388449

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8444092A>T , CM000667.2:g.8444092A>T GRCh38
NC_000005.9:g.8444205A>T , CM000667.1:g.8444205A>T GRCh37
NC_000005.8:g.8497205A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_039984.1:n.174+8131T>A