Canonical Allele Identifier: CA814747112
Gene: LINC02226 HGNC NCBI

Linked Data

dbSNP Id: rs1462299076

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439558T>C , CM000667.2:g.8439558T>C GRCh38
NC_000005.9:g.8439671T>C , CM000667.1:g.8439671T>C GRCh37
NC_000005.8:g.8492671T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039984.1:n.174+12665A>G