Canonical Allele Identifier: CA85231819
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs886817660

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217694T>G , CM000665.2:g.148217694T>G GRCh38
NC_000003.11:g.147935481T>G , CM000665.1:g.147935481T>G GRCh37
NC_000003.10:g.149418171T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2816A>C