Canonical Allele Identifier: CA1543248936
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739804967

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662142T>C , CM000667.2:g.44662142T>C GRCh38
NC_000005.9:g.44662244T>C , CM000667.1:g.44662244T>C GRCh37
NC_000005.8:g.44698001T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3585A>G
XR_925983.1:n.71-3585A>G