Canonical Allele Identifier: CA2199079238
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1342696720
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529597C>T , CM000677.2:g.98529597C>T GRCh38
NC_000015.9:g.99072826C>T , CM000677.1:g.99072826C>T GRCh37
NC_000015.8:g.96890349C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9208G>A
XR_932700.1:n.369-9211G>A
Search 100 bp 5'
Search 100 bp 3'