Canonical Allele Identifier: CA1527043166
Gene: LINC02213 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10512525G= , CM000667.2:g.10512525G= GRCh38
NC_000005.9:g.10512637G= , CM000667.1:g.10512637G= GRCh37
NC_000005.8:g.10565637G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_134289.1:n.330-5950C=