Canonical Allele Identifier: CA1339947233
Gene: LINC01880 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.242084344C= , CM000664.2:g.242084344C= GRCh38
NC_000002.11:g.243026495C= , CM000664.1:g.243026495C= GRCh37
NC_000002.10:g.242675168C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924078.1:n.249G=
XR_924079.1:n.249G=
XR_924080.1:n.249G=
XR_924081.1:n.249G=
XR_924082.1:n.249G=
XR_924083.1:n.249G=
XR_924084.1:n.249G=
XR_924085.1:n.249G=