Canonical Allele Identifier: CA2011125338
Gene: LINC02714 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756933C= , CM000673.2:g.134756933C= GRCh38
NC_000011.9:g.134626827C= , CM000673.1:g.134626827C= GRCh37
NC_000011.8:g.134132037C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4141C=