Canonical Allele Identifier: CA1333499381
Gene: LINC01807 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.228646213T= , CM000664.2:g.228646213T= GRCh38
NC_000002.11:g.229510929T= , CM000664.1:g.229510929T= GRCh37
NC_000002.10:g.229219173T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923977.1:n.39+98430A=