Canonical Allele Identifier: CA2002671880
Gene: LINC02702 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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