Canonical Allele Identifier: CA1543249001
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806320

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662224G>C , CM000667.2:g.44662224G>C GRCh38
NC_000005.9:g.44662326G>C , CM000667.1:g.44662326G>C GRCh37
NC_000005.8:g.44698083G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3667C>G
XR_925983.1:n.71-3667C>G