Canonical Allele Identifier: CA1054734329
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1365583068

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217798T>G , CM000665.2:g.148217798T>G GRCh38
NC_000003.11:g.147935585T>G , CM000665.1:g.147935585T>G GRCh37
NC_000003.10:g.149418275T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2712A>C