Canonical Allele Identifier: CA2046626528
Gene: LINC02882 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.74192380G= , CM000674.2:g.74192380G= GRCh38
NC_000012.11:g.74586160G= , CM000674.1:g.74586160G= GRCh37
NC_000012.10:g.72872427G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038300.1:n.553+1694C=