Canonical Allele Identifier: CA1409673954
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1712869863

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217686T>C , CM000665.2:g.148217686T>C GRCh38
NC_000003.11:g.147935473T>C , CM000665.1:g.147935473T>C GRCh37
NC_000003.10:g.149418163T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2824A>G