Canonical Allele Identifier: CA917032464
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1576573357

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217987_148217988dup , CM000665.2:g.148217987_148217988dup GRCh38
NC_000003.11:g.147935774_147935775dup , CM000665.1:g.147935774_147935775dup GRCh37
NC_000003.10:g.149418464_149418465dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2523_86+2524dup