Canonical Allele Identifier: CA309732156
Gene: LINC01872 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51293045T>C , CM000681.2:g.51293045T>C GRCh38
NC_000019.9:g.51796299T>C , CM000681.1:g.51796299T>C GRCh37
NC_000019.8:g.56488111T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936042.1:n.1771-733T>C
Search 100 bp 5'
Search 100 bp 3'