Canonical Allele Identifier: CA2701763179
Gene: LINC01807 HGNC NCBI

Linked Data

dbSNP Id: rs2106203652

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.228646160G>A , CM000664.2:g.228646160G>A GRCh38
NC_000002.11:g.229510876G>A , CM000664.1:g.229510876G>A GRCh37
NC_000002.10:g.229219120G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923977.1:n.39+98483C>T