Canonical Allele Identifier: CA2199079283
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1897356124

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529688G>T , CM000677.2:g.98529688G>T GRCh38
NC_000015.9:g.99072917G>T , CM000677.1:g.99072917G>T GRCh37
NC_000015.8:g.96890440G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9299C>A
XR_932700.1:n.369-9302C>A