Canonical Allele Identifier: CA14155170
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs12719740

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529676G>A , CM000677.2:g.98529676G>A GRCh38
NC_000015.9:g.99072905G>A , CM000677.1:g.99072905G>A GRCh37
NC_000015.8:g.96890428G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9287C>T
XR_932700.1:n.369-9290C>T