Canonical Allele Identifier: CA1543248999
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806271

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662218C>G , CM000667.2:g.44662218C>G GRCh38
NC_000005.9:g.44662320C>G , CM000667.1:g.44662320C>G GRCh37
NC_000005.8:g.44698077C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3661G>C
XR_925983.1:n.71-3661G>C