Canonical Allele Identifier: CA1054734351
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1712874428

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217864G>T , CM000665.2:g.148217864G>T GRCh38
NC_000003.11:g.147935651G>T , CM000665.1:g.147935651G>T GRCh37
NC_000003.10:g.149418341G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924565.1:n.86+2646C>A