Canonical Allele Identifier: CA973299971

Gene: FAM169BP

Linked Data

• dbSNP Id: rs1897355495
• gnomAD v3: 15-98529616-C-T
• gnomAD v4: 15-98529616-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98529616C>T , CM000677.2:g.98529616C>T	GRCh38
NC_000015.9:g.99072845C>T , CM000677.1:g.99072845C>T	GRCh37
NC_000015.8:g.96890368C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000637259.1:n.575-9227G>A
XR_932700.1:n.369-9230G>A