Canonical Allele Identifier: CA2199079239
Gene: FAM169BP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529597C= , CM000677.2:g.98529597C= GRCh38
NC_000015.9:g.99072826C= , CM000677.1:g.99072826C= GRCh37
NC_000015.8:g.96890349C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9208G=
XR_932700.1:n.369-9211G=