Canonical Allele Identifier: CA1543249389
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739809414

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662506C>G , CM000667.2:g.44662506C>G GRCh38
NC_000005.9:g.44662608C>G , CM000667.1:g.44662608C>G GRCh37
NC_000005.8:g.44698365C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3949G>C
XR_925983.1:n.71-3949G>C