Canonical Allele Identifier: CA275783439
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs925356217

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529690C>T , CM000677.2:g.98529690C>T GRCh38
NC_000015.9:g.99072919C>T , CM000677.1:g.99072919C>T GRCh37
NC_000015.8:g.96890442C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9301G>A
XR_932700.1:n.369-9304G>A