Canonical Allele Identifier: CA229845914
Gene: LINC02698 HGNC NCBI

Linked Data

dbSNP Id: rs638882

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XR_001748394.2:n.469-7409C>T