Canonical Allele Identifier: CA1333499360
Gene: LINC01807 HGNC NCBI

Linked Data

dbSNP Id: rs1696306371

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.228646171G>A , CM000664.2:g.228646171G>A GRCh38
NC_000002.11:g.229510887G>A , CM000664.1:g.229510887G>A GRCh37
NC_000002.10:g.229219131G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923977.1:n.39+98472C>T