Canonical Allele Identifier: CA2765169293
Gene: LINC02145 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324188G>A , CM000667.2:g.6324188G>A GRCh38
NC_000005.9:g.6324301G>A , CM000667.1:g.6324301G>A GRCh37
NC_000005.8:g.6377301G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_028351.1:n.144-11472C>T