Canonical Allele Identifier: CA814747121
Gene: LINC02226 HGNC NCBI

Linked Data

dbSNP Id: rs1199580996

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439561T>A , CM000667.2:g.8439561T>A GRCh38
NC_000005.9:g.8439674T>A , CM000667.1:g.8439674T>A GRCh37
NC_000005.8:g.8492674T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039984.1:n.174+12662A>T