Canonical Allele Identifier: CA1409673931
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1712868963

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217634C>T , CM000665.2:g.148217634C>T GRCh38
NC_000003.11:g.147935421C>T , CM000665.1:g.147935421C>T GRCh37
NC_000003.10:g.149418111C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2876G>A