Canonical Allele Identifier: CA1333499367
Gene: LINC01807 HGNC NCBI

Linked Data

dbSNP Id: rs1696306589

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.228646183A>G , CM000664.2:g.228646183A>G GRCh38
NC_000002.11:g.229510899A>G , CM000664.1:g.229510899A>G GRCh37
NC_000002.10:g.229219143A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923977.1:n.39+98460T>C