Canonical Allele Identifier: CA1409674017
Gene: LINC02045 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217819G= , CM000665.2:g.148217819G= GRCh38
NC_000003.11:g.147935606G= , CM000665.1:g.147935606G= GRCh37
NC_000003.10:g.149418296G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2691C=