Canonical Allele Identifier: CA1526081688
Gene: LINC02226 HGNC NCBI

Linked Data

dbSNP Id: rs1739820989

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439559G>T , CM000667.2:g.8439559G>T GRCh38
NC_000005.9:g.8439672G>T , CM000667.1:g.8439672G>T GRCh37
NC_000005.8:g.8492672G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039984.1:n.174+12664C>A