Canonical Allele Identifier: CA717680023
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1200833483
MyVariant Identifiers: chr15:g.99072926T>A (hg19) chr15:g.98529697T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529697T>A , CM000677.2:g.98529697T>A GRCh38
NC_000015.9:g.99072926T>A , CM000677.1:g.99072926T>A GRCh37
NC_000015.8:g.96890449T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9308A>T
XR_932700.1:n.369-9311A>T
Search 100 bp 5'
Search 100 bp 3'