Canonical Allele Identifier: CA1543249270
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1201362044

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662422G>C , CM000667.2:g.44662422G>C GRCh38
NC_000005.9:g.44662524G>C , CM000667.1:g.44662524G>C GRCh37
NC_000005.8:g.44698281G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3865C>G
XR_925983.1:n.71-3865C>G