Canonical Allele Identifier: CA275783406
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1000914030

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529602G>A , CM000677.2:g.98529602G>A GRCh38
NC_000015.9:g.99072831G>A , CM000677.1:g.99072831G>A GRCh37
NC_000015.8:g.96890354G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9213C>T
XR_932700.1:n.369-9216C>T