Canonical Allele Identifier: CA973299964

Gene: FAM169BP

Linked Data

• dbSNP Id: rs1897355334
• gnomAD v3: 15-98529600-C-G
• gnomAD v4: 15-98529600-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98529600C>G , CM000677.2:g.98529600C>G	GRCh38
NC_000015.9:g.99072829C>G , CM000677.1:g.99072829C>G	GRCh37
NC_000015.8:g.96890352C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000637259.1:n.575-9211G>C
XR_932700.1:n.369-9214G>C