Canonical Allele Identifier: CA2199079232
Gene: FAM169BP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529579G= , CM000677.2:g.98529579G= GRCh38
NC_000015.9:g.99072808G= , CM000677.1:g.99072808G= GRCh37
NC_000015.8:g.96890331G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9190C=
XR_932700.1:n.369-9193C=