Canonical Allele Identifier: CA717679956
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1478925990

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529615C>A , CM000677.2:g.98529615C>A GRCh38
NC_000015.9:g.99072844C>A , CM000677.1:g.99072844C>A GRCh37
NC_000015.8:g.96890367C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9226G>T
XR_932700.1:n.369-9229G>T