Canonical Allele Identifier: CA337136711
Gene: STSP1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.15551598G>T
GRCh37 chrY:g.17663478G>T
gnomAD v4:
chrY-15551598-G-T
Joint Max Group AF 0.03361657 (EAS)
Exomes Max Group AF 0.05011293 (EAS)
dbSNP:
35557642
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15551598G>T , CM000686.2:g.15551598G>T GRCh38
NC_000024.9:g.17663478G>T , CM000686.1:g.17663478G>T GRCh37
NC_000024.8:g.16172872G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000412493.1:n.476G>T
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