Canonical Allele Identifier: CA1409673941
Gene: LINC02045 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217649A= , CM000665.2:g.148217649A= GRCh38
NC_000003.11:g.147935436A= , CM000665.1:g.147935436A= GRCh37
NC_000003.10:g.149418126A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2861T=