Canonical Allele Identifier: CA1543249069
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739807053

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662302A>G , CM000667.2:g.44662302A>G GRCh38
NC_000005.9:g.44662404A>G , CM000667.1:g.44662404A>G GRCh37
NC_000005.8:g.44698161A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3745T>C
XR_925983.1:n.71-3745T>C