Canonical Allele Identifier: CA2838014152
Gene: LINC02702 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116649810G>A , CM000673.2:g.116649810G>A GRCh38
NC_000011.9:g.116520527G>A , CM000673.1:g.116520527G>A GRCh37
NC_000011.8:g.116025737G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_135069.1:n.117-3088G>A
XR_246484.2:n.117-3088G>A
XR_948058.1:n.100-3088G>A