Canonical Allele Identifier: CA337136581
Gene: STSP1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.15549506G>A
GRCh37 chrY:g.17661386G>A
gnomAD v4:
chrY-15549506-G-A
Joint Max Group AF 0.08740142 (SAS)
Exomes Max Group AF 0.09915859 (SAS)
dbSNP:
72625377
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15549506G>A , CM000686.2:g.15549506G>A GRCh38
NC_000024.9:g.17661386G>A , CM000686.1:g.17661386G>A GRCh37
NC_000024.8:g.16170780G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000412493.1:n.144-105G>A
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