Canonical Allele Identifier: CA16239538
Gene: LINC02147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118002058G>A , CM000667.2:g.118002058G>A GRCh38
NC_000005.9:g.117337753G>A , CM000667.1:g.117337753G>A GRCh37
NC_000005.8:g.117365652G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104997.1:n.170+76927G>A