Canonical Allele Identifier: CA337725469
Gene: SFPQP1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.13090694C>G
gnomAD v3:
Y:13090694 C / G
gnomAD v4:
chrY-13090694-C-G
Joint Max Group AF 0.93681043 (EAS)
Genomes Max Group AF 0.93681043 (EAS)
dbSNP:
2191146
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13090694C>G , CM000686.2:g.13090694C>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000446621.1:n.556-3881C>G
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