Canonical Allele Identifier: CA2199079244
Gene: FAM169BP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529603T= , CM000677.2:g.98529603T= GRCh38
NC_000015.9:g.99072832T= , CM000677.1:g.99072832T= GRCh37
NC_000015.8:g.96890355T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9214A=
XR_932700.1:n.369-9217A=