Canonical Allele Identifier: CA1140011927
Gene: LINC01707 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.69113569G= , CM000663.2:g.69113569G= GRCh38
NC_000001.10:g.69579252G= , CM000663.1:g.69579252G= GRCh37
NC_000001.9:g.69351840G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947481.1:n.303+28271G=
XR_947482.1:n.303+28271G=
NR_146608.1:n.317+25007G=