Canonical Allele Identifier: CA1409673948
Gene: LINC02045 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217674C= , CM000665.2:g.148217674C= GRCh38
NC_000003.11:g.147935461C= , CM000665.1:g.147935461C= GRCh37
NC_000003.10:g.149418151C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2836G=