Canonical Allele Identifier: CA717679932
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1342696720
MyVariant Identifiers: chr15:g.99072826C>A (hg19) chr15:g.98529597C>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9208G>T
XR_932700.1:n.369-9211G>T
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