Canonical Allele Identifier: CA2805405337
Gene: FAM169BP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529614T>A , CM000677.2:g.98529614T>A GRCh38
NC_000015.9:g.99072843T>A , CM000677.1:g.99072843T>A GRCh37
NC_000015.8:g.96890366T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9225A>T
XR_932700.1:n.369-9228A>T