Canonical Allele Identifier: CA2046626518
Gene: LINC02882 HGNC NCBI

Linked Data

dbSNP Id: rs1874570434

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.74192372T>C , CM000674.2:g.74192372T>C GRCh38
NC_000012.11:g.74586152T>C , CM000674.1:g.74586152T>C GRCh37
NC_000012.10:g.72872419T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038300.1:n.553+1702A>G