Canonical Allele Identifier: CA1952245208
Gene: LINC02752 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.11206827C>T , CM000673.2:g.11206827C>T GRCh38
NC_000011.9:g.11228374C>T , CM000673.1:g.11228374C>T GRCh37
NC_000011.8:g.11184950C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748132.1:n.3406-21252C>T