Canonical Allele Identifier: CA2046626577
Community Standard Title: NC_000012.12:g.74192430T=
Gene: LINC02882 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.74192430T= , CM000674.2:g.74192430T= GRCh38
NC_000012.11:g.74586210T= , CM000674.1:g.74586210T= GRCh37
NC_000012.10:g.72872477T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038300.1:n.553+1644A=