Canonical Allele Identifier: CA85231872
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1035091823

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217894A>G , CM000665.2:g.148217894A>G GRCh38
NC_000003.11:g.147935681A>G , CM000665.1:g.147935681A>G GRCh37
NC_000003.10:g.149418371A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2616T>C