Canonical Allele Identifier: CA1054734259
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1041835687

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217611C>A , CM000665.2:g.148217611C>A GRCh38
NC_000003.11:g.147935398C>A , CM000665.1:g.147935398C>A GRCh37
NC_000003.10:g.149418088C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2899G>T