Canonical Allele Identifier: CA2599046555
Gene: FAM169BP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529682C>G , CM000677.2:g.98529682C>G GRCh38
NC_000015.9:g.99072911C>G , CM000677.1:g.99072911C>G GRCh37
NC_000015.8:g.96890434C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9293G>C
XR_932700.1:n.369-9296G>C