Canonical Allele Identifier: CA1543249017
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806492

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662239T>C , CM000667.2:g.44662239T>C GRCh38
NC_000005.9:g.44662341T>C , CM000667.1:g.44662341T>C GRCh37
NC_000005.8:g.44698098T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3682A>G
XR_925983.1:n.71-3682A>G