Canonical Allele Identifier: CA1409674043
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1712874503

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217866T>C , CM000665.2:g.148217866T>C GRCh38
NC_000003.11:g.147935653T>C , CM000665.1:g.147935653T>C GRCh37
NC_000003.10:g.149418343T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924565.1:n.86+2644A>G