Canonical Allele Identifier: CA85231825
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs570967941

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217746A>G , CM000665.2:g.148217746A>G GRCh38
NC_000003.11:g.147935533A>G , CM000665.1:g.147935533A>G GRCh37
NC_000003.10:g.149418223A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2764T>C