Canonical Allele Identifier: CA130382749
Gene: LINC01861 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.153960408C>G , CM000667.2:g.153960408C>G GRCh38
NC_000005.9:g.153339968C>G , CM000667.1:g.153339968C>G GRCh37
NC_000005.8:g.153320161C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944434.1:n.381+15279G>C
XR_001742937.1:n.124-5940G>C