Canonical Allele Identifier: CA2708011219
Gene: LINC02515 HGNC NCBI

Linked Data

dbSNP Id: rs2111131120

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.187424173T>C , CM000666.2:g.187424173T>C GRCh38
NC_000004.11:g.188345327T>C , CM000666.1:g.188345327T>C GRCh37
NC_000004.10:g.188582321T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038931.1:n.322+81119A>G
XR_939603.1:n.268+1176T>C
XR_001741954.1:n.258+10462T>C
XR_001741955.1:n.1517+1176T>C
XR_001741956.1:n.258+10462T>C
XR_939603.2:n.269+1176T>C