Canonical Allele Identifier: CA2225765507
Gene: LINC02141 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.59906284T>A , CM000678.2:g.59906284T>A GRCh38
NC_000016.9:g.59940188T>A , CM000678.1:g.59940188T>A GRCh37
NC_000016.8:g.58497689T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110917.1:n.173+50759T>A