Canonical Allele Identifier: CA2192801808
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs1416957254

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756812T>C , CM000677.2:g.85756812T>C GRCh38
NC_000015.9:g.86300043T>C , CM000677.1:g.86300043T>C GRCh37
NC_000015.8:g.84101047T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.420-856A>G