Canonical Allele Identifier: CA1525089266
Gene: LINC02145 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324088A= , CM000667.2:g.6324088A= GRCh38
NC_000005.9:g.6324201A= , CM000667.1:g.6324201A= GRCh37
NC_000005.8:g.6377201A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11372T=