Canonical Allele Identifier: CA1520487886
Gene: LINC02515 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.187424125A= , CM000666.2:g.187424125A= GRCh38
NC_000004.11:g.188345279A= , CM000666.1:g.188345279A= GRCh37
NC_000004.10:g.188582273A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038931.1:n.322+81167T=
XR_939603.1:n.268+1128A=
XR_001741954.1:n.258+10414A=
XR_001741955.1:n.1517+1128A=
XR_001741956.1:n.258+10414A=
XR_939603.2:n.269+1128A=