Canonical Allele Identifier: CA1543249395
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739809525

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662542T>G , CM000667.2:g.44662542T>G GRCh38
NC_000005.9:g.44662644T>G , CM000667.1:g.44662644T>G GRCh37
NC_000005.8:g.44698401T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3985A>C
XR_925983.1:n.71-3985A>C