Canonical Allele Identifier: CA337137372
Gene: STSP1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.15566923G>A
GRCh37 chrY:g.17678803G>A
gnomAD v4:
chrY-15566923-G-A
Joint Max Group AF 0.00002131 (SAS)
Exomes Max Group AF 0.00002337 (SAS)
dbSNP:
35852845
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15566923G>A , CM000686.2:g.15566923G>A GRCh38
NC_000024.9:g.17678803G>A , CM000686.1:g.17678803G>A GRCh37
NC_000024.8:g.16188197G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000412493.1:n.1045G>A
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