Canonical Allele Identifier: CA337137811
Gene: STSP1 HGNC NCBI

Linked Data

dbSNP Id: rs760407622
MyVariant Identifiers: chrY:g.17684699A>T (hg19) chrY:g.15572819A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15572819A>T , CM000686.2:g.15572819A>T GRCh38
NC_000024.9:g.17684699A>T , CM000686.1:g.17684699A>T GRCh37
NC_000024.8:g.16194093A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000412493.1:n.1050+5891A>T
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