Canonical Allele Identifier: CA2199079240
Gene: FAM169BP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529598A= , CM000677.2:g.98529598A= GRCh38
NC_000015.9:g.99072827A= , CM000677.1:g.99072827A= GRCh37
NC_000015.8:g.96890350A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9209T=
XR_932700.1:n.369-9212T=