Canonical Allele Identifier: CA337137820
Gene: STSP1 HGNC NCBI

Linked Data

dbSNP Id: rs557770144
MyVariant Identifiers: chrY:g.17684724A>G (hg19) chrY:g.15572844A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15572844A>G , CM000686.2:g.15572844A>G GRCh38
NC_000024.9:g.17684724A>G , CM000686.1:g.17684724A>G GRCh37
NC_000024.8:g.16194118A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000412493.1:n.1050+5916A>G
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