Canonical Allele Identifier: CA1512203964
Gene: LINC02275 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.169959732G= , CM000666.2:g.169959732G= GRCh38
NC_000004.11:g.170880883G= , CM000666.1:g.170880883G= GRCh37
NC_000004.10:g.171117458G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037878.1:n.87+16084C=