Canonical Allele Identifier: CA1409673981
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1712870754

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217750C>T , CM000665.2:g.148217750C>T GRCh38
NC_000003.11:g.147935537C>T , CM000665.1:g.147935537C>T GRCh37
NC_000003.10:g.149418227C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2760G>A