Canonical Allele Identifier: CA717679941
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1316723731

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529598A>C , CM000677.2:g.98529598A>C GRCh38
NC_000015.9:g.99072827A>C , CM000677.1:g.99072827A>C GRCh37
NC_000015.8:g.96890350A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9209T>G
XR_932700.1:n.369-9212T>G