Canonical Allele Identifier: CA1520487899
Gene: LINC02515 HGNC NCBI

Linked Data

dbSNP Id: rs1735027631

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.187424148T>C , CM000666.2:g.187424148T>C GRCh38
NC_000004.11:g.188345302T>C , CM000666.1:g.188345302T>C GRCh37
NC_000004.10:g.188582296T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038931.1:n.322+81144A>G
XR_939603.1:n.268+1151T>C
XR_001741954.1:n.258+10437T>C
XR_001741955.1:n.1517+1151T>C
XR_001741956.1:n.258+10437T>C
XR_939603.2:n.269+1151T>C