Canonical Allele Identifier: CA1543248985
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806094

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662207A>T , CM000667.2:g.44662207A>T GRCh38
NC_000005.9:g.44662309A>T , CM000667.1:g.44662309A>T GRCh37
NC_000005.8:g.44698066A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3650T>A
XR_925983.1:n.71-3650T>A