Canonical Allele Identifier: CA792439278
Gene: LINC02515 HGNC NCBI

Linked Data

dbSNP Id: rs1360386286

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.187424145C>G , CM000666.2:g.187424145C>G GRCh38
NC_000004.11:g.188345299C>G , CM000666.1:g.188345299C>G GRCh37
NC_000004.10:g.188582293C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038931.1:n.322+81147G>C
XR_939603.1:n.268+1148C>G
XR_001741954.1:n.258+10434C>G
XR_001741955.1:n.1517+1148C>G
XR_001741956.1:n.258+10434C>G
XR_939603.2:n.269+1148C>G