Canonical Allele Identifier: CA2199079299
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1270528667

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529726G>C , CM000677.2:g.98529726G>C GRCh38
NC_000015.9:g.99072955G>C , CM000677.1:g.99072955G>C GRCh37
NC_000015.8:g.96890478G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637259.1:n.575-9337C>G
XR_932700.1:n.369-9340C>G