Canonical Allele Identifier: CA13398238
Gene: LINC02702 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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