Canonical Allele Identifier: CA811039898
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1219876683

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662301_44662303del , CM000667.2:g.44662301_44662303del GRCh38
NC_000005.9:g.44662403_44662405del , CM000667.1:g.44662403_44662405del GRCh37
NC_000005.8:g.44698160_44698162del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3745_92-3743del
XR_925983.1:n.71-3745_71-3743del