Canonical Allele Identifier: CA1543249203
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739808014

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662382T>C , CM000667.2:g.44662382T>C GRCh38
NC_000005.9:g.44662484T>C , CM000667.1:g.44662484T>C GRCh37
NC_000005.8:g.44698241T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3825A>G
XR_925983.1:n.71-3825A>G