Canonical Allele Identifier: CA880350189
Gene: STSP1 HGNC NCBI

Linked Data

dbSNP Id: rs1287952098
MyVariant Identifiers: chrY:g.17684801T>A (hg19) chrY:g.15572921T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15572921T>A , CM000686.2:g.15572921T>A GRCh38
NC_000024.9:g.17684801T>A , CM000686.1:g.17684801T>A GRCh37
NC_000024.8:g.16194195T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000412493.1:n.1050+5993T>A
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