Canonical Allele Identifier: CA1520487888
Gene: LINC02515 HGNC NCBI

Linked Data

dbSNP Id: rs1735027344

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.187424130T>C , CM000666.2:g.187424130T>C GRCh38
NC_000004.11:g.188345284T>C , CM000666.1:g.188345284T>C GRCh37
NC_000004.10:g.188582278T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038931.1:n.322+81162A>G
XR_939603.1:n.268+1133T>C
XR_001741954.1:n.258+10419T>C
XR_001741955.1:n.1517+1133T>C
XR_001741956.1:n.258+10419T>C
XR_939603.2:n.269+1133T>C