Canonical Allele Identifier: CA1543249177
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739807772

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662366C>G , CM000667.2:g.44662366C>G GRCh38
NC_000005.9:g.44662468C>G , CM000667.1:g.44662468C>G GRCh37
NC_000005.8:g.44698225C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3809G>C
XR_925983.1:n.71-3809G>C