Canonical Allele Identifier: CA337137368
Gene: STSP1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.15566813A>G
GRCh37 chrY:g.17678693A>G
gnomAD v4:
chrY-15566813-A-G
Joint Max Group AF 0.21146173 (AFR)
Exomes Max Group AF 0.59987853 (AFR)
dbSNP:
9786326
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15566813A>G , CM000686.2:g.15566813A>G GRCh38
NC_000024.9:g.17678693A>G , CM000686.1:g.17678693A>G GRCh37
NC_000024.8:g.16188087A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000412493.1:n.935A>G
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