Canonical Allele Identifier: CA2199079252
Gene: FAM169BP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529623C= , CM000677.2:g.98529623C= GRCh38
NC_000015.9:g.99072852C= , CM000677.1:g.99072852C= GRCh37
NC_000015.8:g.96890375C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9234G=
XR_932700.1:n.369-9237G=