Canonical Allele Identifier: CA1525089332
Gene: LINC02145 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324252A= , CM000667.2:g.6324252A= GRCh38
NC_000005.9:g.6324365A= , CM000667.1:g.6324365A= GRCh37
NC_000005.8:g.6377365A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11536T=