Canonical Allele Identifier: CA85231868
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs144159670

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217889T>G , CM000665.2:g.148217889T>G GRCh38
NC_000003.11:g.147935676T>G , CM000665.1:g.147935676T>G GRCh37
NC_000003.10:g.149418366T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924565.1:n.86+2621A>C