Canonical Allele Identifier: CA337137006
Gene: STSP1 HGNC NCBI

Linked Data

dbSNP Id: rs112486787
MyVariant Identifiers: chrY:g.17670179T>C (hg19) chrY:g.15558299T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15558299T>C , CM000686.2:g.15558299T>C GRCh38
NC_000024.9:g.17670179T>C , CM000686.1:g.17670179T>C GRCh37
NC_000024.8:g.16179573T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000412493.1:n.893+6284T>C
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