Canonical Allele Identifier: CA275783411
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs79693444

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529610C>T , CM000677.2:g.98529610C>T GRCh38
NC_000015.9:g.99072839C>T , CM000677.1:g.99072839C>T GRCh37
NC_000015.8:g.96890362C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9221G>A
XR_932700.1:n.369-9224G>A