Canonical Allele Identifier: CA2199079251
Gene: FAM169BP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529620G= , CM000677.2:g.98529620G= GRCh38
NC_000015.9:g.99072849G= , CM000677.1:g.99072849G= GRCh37
NC_000015.8:g.96890372G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9231C=
XR_932700.1:n.369-9234C=