Canonical Allele Identifier: CA1409674059
Gene: LINC02045 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217890A= , CM000665.2:g.148217890A= GRCh38
NC_000003.11:g.147935677A= , CM000665.1:g.147935677A= GRCh37
NC_000003.10:g.149418367A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924565.1:n.86+2620T=