Canonical Allele Identifier: CA1054734310
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1712870508

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217728G>A , CM000665.2:g.148217728G>A GRCh38
NC_000003.11:g.147935515G>A , CM000665.1:g.147935515G>A GRCh37
NC_000003.10:g.149418205G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2782C>T