Canonical Allele Identifier: CA973300009
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1200833483
gnomAD v3: 15-98529697-T-C
gnomAD v4: 15-98529697-T-C
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9308A>G
XR_932700.1:n.369-9311A>G
Search 100 bp 5'
Search 100 bp 3'