Canonical Allele Identifier: CA1072075434
Gene: LINC02515 HGNC NCBI

Linked Data

dbSNP Id: rs1735028045

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.187424176C>G , CM000666.2:g.187424176C>G GRCh38
NC_000004.11:g.188345330C>G , CM000666.1:g.188345330C>G GRCh37
NC_000004.10:g.188582324C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038931.1:n.322+81116G>C
XR_939603.1:n.268+1179C>G
XR_001741954.1:n.258+10465C>G
XR_001741955.1:n.1517+1179C>G
XR_001741956.1:n.258+10465C>G
XR_939603.2:n.269+1179C>G