Canonical Allele Identifier: CA1520487900
Gene: LINC02515 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.187424151C= , CM000666.2:g.187424151C= GRCh38
NC_000004.11:g.188345305C= , CM000666.1:g.188345305C= GRCh37
NC_000004.10:g.188582299C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038931.1:n.322+81141G=
XR_939603.1:n.268+1154C=
XR_001741954.1:n.258+10440C=
XR_001741955.1:n.1517+1154C=
XR_001741956.1:n.258+10440C=
XR_939603.2:n.269+1154C=