Canonical Allele Identifier: CA14380019
Gene: LINC02086 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48672429A>C , CM000679.2:g.48672429A>C GRCh38
NC_000017.10:g.46749791A>C , CM000679.1:g.46749791A>C GRCh37
NC_000017.9:g.44104790A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934812.1:n.768-10830A>C
XR_934813.1:n.768-10810A>C
XR_934814.1:n.611-10830A>C
XR_934815.1:n.232-10830A>C
XR_934817.1:n.610-10830A>C
XR_934819.1:n.776-10830A>C
XR_001752925.2:n.38-10830A>C