Canonical Allele Identifier: CA2002310785
Gene: LINC02698 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.115893327C= , CM000673.2:g.115893327C= GRCh38
NC_000011.9:g.115764045C= , CM000673.1:g.115764045C= GRCh37
NC_000011.8:g.115269255C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748394.2:n.469-7409C=