Canonical Allele Identifier: CA229845914
Gene: LINC02698 HGNC NCBI
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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
Search 100 bp 5'
Search 100 bp 3'