Canonical Allele Identifier: CA1525089314
Gene: LINC02145 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324189C= , CM000667.2:g.6324189C= GRCh38
NC_000005.9:g.6324302C= , CM000667.1:g.6324302C= GRCh37
NC_000005.8:g.6377302C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11473G=