Canonical Allele Identifier: CA1242881822
Gene: LINC00486 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32896437A= , CM000664.2:g.32896437A= GRCh38
NC_000002.11:g.33121504A= , CM000664.1:g.33121504A= GRCh37
NC_000002.10:g.32975008A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027098.1:n.290-2103A=
NR_027099.1:n.253-488A=
NR_027100.1:n.27-2103A=
XR_939938.1:n.351+6300T=
XR_939939.1:n.39-6439T=
NR_027098.2:n.300-2103A=
NR_027099.2:n.968-488A=
XR_939938.2:n.354+6300T=