Canonical Allele Identifier: CA2391929894
Gene: LINC00163 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44993730A= , CM000683.2:g.44993730A= GRCh38
NC_000021.8:g.46413645A= , CM000683.1:g.46413645A= GRCh37
NC_000021.7:g.45238073A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033840.1:n.183+174T=