Canonical Allele Identifier: CA337725514
Gene: SFPQP1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.13092794T>G
gnomAD v3:
Y:13092794 T / G
gnomAD v4:
chrY-13092794-T-G
Joint Max Group AF 0.12495 (MID)
Genomes Max Group AF 0.04989553 (AMR)
dbSNP:
9785723
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13092794T>G , CM000686.2:g.13092794T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000446621.1:n.556-1781T>G
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