Canonical Allele Identifier: CA275783446

Gene: FAM169BP

Linked Data

• dbSNP Id: rs944586653
• gnomAD v3: 15-98529720-C-A
• gnomAD v4: 15-98529720-C-A
• MyVariant Identifiers: chr15:g.99072949C>A (hg19) ; chr15:g.98529720C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98529720C>A , CM000677.2:g.98529720C>A	GRCh38
NC_000015.9:g.99072949C>A , CM000677.1:g.99072949C>A	GRCh37
NC_000015.8:g.96890472C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000637259.1:n.575-9331G>T
XR_932700.1:n.369-9334G>T