Canonical Allele Identifier: CA717679946
Gene: FAM169BP HGNC NCBI

Linked Data

dbSNP Id: rs1295330644
MyVariant Identifiers: chr15:g.99072832T>C (hg19) chr15:g.98529603T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98529603T>C , CM000677.2:g.98529603T>C GRCh38
NC_000015.9:g.99072832T>C , CM000677.1:g.99072832T>C GRCh37
NC_000015.8:g.96890355T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000637259.1:n.575-9214A>G
XR_932700.1:n.369-9217A>G
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