Canonical Allele Identifier: CA15842826
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs62025270

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756967G>A , CM000677.2:g.85756967G>A GRCh38
NC_000015.9:g.86300198G>A , CM000677.1:g.86300198G>A GRCh37
NC_000015.8:g.84101202G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120366.1:n.419+917C>T