Canonical Allele Identifier: CA113946462
Gene: LINC02226 HGNC NCBI

Linked Data

dbSNP Id: rs939497655

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439598G>A , CM000667.2:g.8439598G>A GRCh38
NC_000005.9:g.8439711G>A , CM000667.1:g.8439711G>A GRCh37
NC_000005.8:g.8492711G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039984.1:n.174+12625C>T