Canonical Allele Identifier: CA275783409
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs752208801
gnomAD v2: 15-99072837-C-T
gnomAD v3: 15-98529608-C-T
gnomAD v4: 15-98529608-C-T
MyVariant Identifiers: chr15:g.99072837C>T (hg19) chr15:g.98529608C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529608C>T , CM000677.2:g.98529608C>T GRCh38
NC_000015.9:g.99072837C>T , CM000677.1:g.99072837C>T GRCh37
NC_000015.8:g.96890360C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9219G>A
XR_932700.1:n.369-9222G>A
Search 100 bp 5'
Search 100 bp 3'