Canonical Allele Identifier: CA948920898
Gene: LINC02373 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69433878G>A , CM000674.2:g.69433878G>A GRCh38
NC_000012.11:g.69827658G>A , CM000674.1:g.69827658G>A GRCh37
NC_000012.10:g.68113925G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945061.1:n.163+2165G>A