ClinGen Allele Registry
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Canonical Allele Identifier:
CA337138234
Gene: STSP1
HGNC
NCBI
Linked Data
dbSNP Id:
rs112174873
MyVariant Identifiers:
chrY:g.17692832G>A (hg19)
chrY:g.15580952G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.15580952G>A , CM000686.2:g.15580952G>A
GRCh38
NC_000024.9:g.17692832G>A , CM000686.1:g.17692832G>A
GRCh37
NC_000024.8:g.16202226G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000412493.1:n.1051-12279G>A
Search 100 bp 5'
Search 100 bp 3'